Canonical Allele Identifier: PA658680820
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys692Arg
CA46710290
NM_000179.3:c.2075A>G