Canonical Allele Identifier: PA331559
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91041
ClinVar RCV Id: RCV000221964 RCV000412138 RCV000552261 RCV001353838 RCV001196697 RCV003387753 RCV003997169
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu92Val
CA020916
NM_000251.3:c.274C>G