Canonical Allele Identifier: PA195905
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 186799
ClinVar RCV Id: RCV000166449 RCV001296242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln10His
CA021004
NM_000251.3:c.30G>T
CA346728488
NM_000251.3:c.30G>C