Canonical Allele Identifier: PA287342
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127604

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu228Lys
CA016246
NM_000179.3:c.682G>A