Canonical Allele Identifier: PA2499230107
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1039589
ClinVar RCV Id: RCV001343087

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr594Ala
CA031253
NM_000251.3:c.1780A>G