Canonical Allele Identifier: PA2825089980
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1794632
ClinVar RCV Id: RCV002428866

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu893Arg
CA346755275
NM_000179.3:c.2678T>G