Canonical Allele Identifier: PA2826629518
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 855477

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser7Pro
CA346740748
NM_001281493.2:c.19T>C