Canonical Allele Identifier: PA095569
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 99033
ClinVar RCV Id: RCV000085376 RCV001096640 RCV000764205 RCV000986372 RCV001073759 RCV001257823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000341.2:p.Asn380Lys
CA226872
NM_000350.3:c.1140T>A
CA341283450
NM_000350.3:c.1140T>G