Canonical Allele Identifier: PA104853
Gene: ABCA12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775099.2:p.Gly1651Ser
CA252476
NM_173076.3:c.4951G>A