Canonical Allele Identifier: PA331670
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1758545
ClinVar RCV Id: RCV002380341

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys246Gln
CA022120
NM_000251.3:c.736A>C