Canonical Allele Identifier: PA2826630792
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ile306Thr
CA346749466
NM_001281493.2:c.917T>C