Canonical Allele Identifier: PA226930
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 99082
ClinVar RCV Id: RCV000085426
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000341.2:p.Asp600Tyr
CA226929
NM_000350.3:c.1798G>T