Canonical Allele Identifier: PA2826635995
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184444

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr462Asn
CA009966
NM_001281494.2:c.1385C>A