Canonical Allele Identifier: PA191560
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 185297
ClinVar RCV Id: RCV000164692 RCV000228123 RCV000235224 RCV000412025 RCV001374485 RCV003226226 RCV003993847 RCV003995359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro27Leu
CA022338
NM_000251.3:c.80C>T