Canonical Allele Identifier: PA2579912723
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3076127
ClinVar RCV Id: RCV004018444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asp236Tyr
CA346732029
NM_000251.3:c.706G>T