Canonical Allele Identifier: PA334710
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 188356
ClinVar RCV Id: RCV000168388 RCV000508172 RCV000568410 RCV003468832 RCV003995625
ClinVar Variation Id: 408521
ClinVar RCV Id: RCV000470314 RCV000491232 RCV003329284 RCV003153620
ClinVar Variation Id: 570175
ClinVar RCV Id: RCV000690977 RCV002397393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Phe58Leu
CA019166
NM_000251.3:c.174C>A
CA030766
NM_000251.3:c.174C>G
CA346728992
NM_000251.3:c.172T>C