Canonical Allele Identifier: PA645474711
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418316

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asp603His
CA16617590
NM_000251.3:c.1807G>C