Canonical Allele Identifier: PA2825092656
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1714899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala1306Thr
CA346761452
NM_000179.3:c.3916G>A