Canonical Allele Identifier: PA188987
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr764Asn
CA009966
NM_000179.3:c.2291C>A