Canonical Allele Identifier: PA913193552
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 631206
ClinVar Variation Id: 844004
ClinVar RCV Id: RCV001046744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met894Leu
CA346731528
NM_000251.3:c.2680A>C
CA346731533
NM_000251.3:c.2680A>T