Canonical Allele Identifier: PA645439477
Gene: ABCA12 HGNC NCBI

Linked Data

ClinVar Variation Id: 334256
ClinVar RCV Id: RCV000284106
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775099.2:p.Thr759Ser
CA10614259
NM_173076.3:c.2276C>G
CA350483505
NM_173076.3:c.2275A>T