Canonical Allele Identifier: PA645378768
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 230984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg240Gln
CA073373
NM_000179.3:c.719G>A