Canonical Allele Identifier: PA2826631466
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr462Asn
CA009966
NM_001281493.2:c.1385C>A