Canonical Allele Identifier: PA2826636124
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790403

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp491Glu
CA346753736
NM_001281494.2:c.1473T>A
CA346753739
NM_001281494.2:c.1473T>G