Canonical Allele Identifier: PA2825089702
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1791544
ClinVar RCV Id: RCV002450539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu819Lys
CA346754076
NM_000179.3:c.2455G>A