Canonical Allele Identifier: PA658672442
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486884
ClinVar RCV Id: RCV000575075 RCV001302760
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg482Thr
CA346726916
NM_000251.3:c.1445G>C