Canonical Allele Identifier: PA2825089417
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1788889

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu760Lys
CA346752868
NM_000179.3:c.2278G>A