Canonical Allele Identifier: PA645476434
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237393
ClinVar RCV Id: RCV000565937 RCV000663160 RCV000485086 RCV000231382 RCV000781561
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile926Asn
CA037530
NM_000251.3:c.2777T>A