Canonical Allele Identifier: PA2825086768
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2008181
ClinVar RCV Id: RCV002833678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val250Asp
CA346740120
NM_000179.3:c.749T>A