Canonical Allele Identifier: PA2499230013
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1007418
ClinVar RCV Id: RCV001304598 RCV002411970
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu260Lys
CA346732458
NM_000251.3:c.778G>A