Canonical Allele Identifier: PA2826629621
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1768617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser29Thr
CA346741104
NM_001281493.2:c.85T>A