Canonical Allele Identifier: PA2826632463
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu693Lys
CA10578125
NM_001281493.2:c.2077G>A