Canonical Allele Identifier: PA645472486
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418314
ClinVar RCV Id: RCV000480961 RCV000558255 RCV000566262 RCV000656874 RCV001250426
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val273Ala
CA040789
NM_000251.3:c.818T>C