Canonical Allele Identifier: PA2579910548
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1729820
ClinVar RCV Id: RCV002445814
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys110Glu
CA346729991
NM_000251.3:c.328A>G