Canonical Allele Identifier: PA1139681937
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 838884
ClinVar RCV Id: RCV001040531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala848Val
CA346730846
NM_000251.3:c.2543C>T