Canonical Allele Identifier: PA2826465473
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1789918
ClinVar RCV Id: RCV002428532 RCV003759726
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Thr716Ile
CA346729951
NM_001258281.1:c.2147C>T