Canonical Allele Identifier: PA2830355393
Gene: ABCA12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2313958
ClinVar RCV Id: RCV002897111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775099.2:p.Phe1111Leu
CA350469658
NM_173076.3:c.3333C>G
CA350469659
NM_173076.3:c.3333C>A
CA350469668
NM_173076.3:c.3331T>C