Canonical Allele Identifier: PA645439355
Gene: ABCA12 HGNC NCBI

Linked Data

ClinVar Variation Id: 388614

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775099.2:p.Arg44Trp
CA2092660
NM_173076.3:c.130C>T