Canonical Allele Identifier: PA2826627118
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr634Asn
CA009966
NM_001281492.2:c.1901C>A