Canonical Allele Identifier: PA104819
Gene: ABCA12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2863
ClinVar RCV Id: RCV000002997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775099.2:p.Gly1179Arg
CA252486
NM_173076.3:c.3535G>A
CA350468560
NM_173076.3:c.3535G>C