Canonical Allele Identifier: PA2579909034
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230848
ClinVar RCV Id: RCV004522962
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly18Ser
CA346728572
NM_000251.3:c.52G>A