Canonical Allele Identifier: PA2826464930
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237379
ClinVar RCV Id: RCV000226382 RCV001013729 RCV003998759
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile585Val
CA10582019
NM_001258281.1:c.1753A>G