Canonical Allele Identifier: PA2826635965
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2676802
ClinVar RCV Id: RCV003461939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr455Ala
CA346752811
NM_001281494.2:c.1363A>G