Canonical Allele Identifier: PA2573164920
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1473785
ClinVar RCV Id: RCV001970864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asn263Tyr
CA346732507
NM_000251.3:c.787A>T