Canonical Allele Identifier: PA2826631468
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1049172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr462Ser
CA10654940
NM_001281493.2:c.1385C>G
CA346752960
NM_001281493.2:c.1384A>T