Canonical Allele Identifier: PA916065641
Gene: ABCA12 HGNC NCBI

Linked Data

ClinVar Variation Id: 791887
ClinVar RCV Id: RCV000974943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775099.2:p.Ser777Phe
CA2091992
NM_173076.3:c.2330C>T