Canonical Allele Identifier: PA2826465907
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_001245210.1:p.Met828Leu
CA346731528
NM_001258281.1:c.2482A>C
CA346731533
NM_001258281.1:c.2482A>T