Canonical Allele Identifier: PA2573165111
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1511034

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.His665Pro
CA346728927
NM_000251.3:c.1994A>C