Canonical Allele Identifier: PA113188
Gene: SIX6 HGNC NCBI

Linked Data

ClinVar Variation Id: 4436
ClinVar RCV Id: RCV000004686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_031400.2:p.Thr165Ala
CA214925
NM_007374.3:c.493A>G