Canonical Allele Identifier: PA2826631587
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 229774

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg489His
CA068883
NM_001281493.2:c.1466G>A