Canonical Allele Identifier: PA2826463871
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408525
ClinVar RCV Id: RCV000473029 RCV001535616 RCV002329043 RCV003463908
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys326Met
CA027158
NM_001258281.1:c.977A>T