Canonical Allele Identifier: PA191087
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 185118
ClinVar RCV Id: RCV000164484 RCV002516464
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met261Leu
CA022236
NM_000251.3:c.781A>T
CA346732471
NM_000251.3:c.781A>C