Canonical Allele Identifier: PA164697
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val606Asp
CA019381
NM_000251.3:c.1817T>A