Canonical Allele Identifier: PA658739536
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 489938
ClinVar RCV Id: RCV000580054 RCV001229080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val817Met
CA346730299
NM_000251.3:c.2449G>A