Canonical Allele Identifier: PA357558
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 219668

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu602Val
CA031475
NM_000251.3:c.1804C>G