Canonical Allele Identifier: PA226959
Gene: ABCA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 99102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000341.2:p.Val643Gly
CA226958
NM_000350.3:c.1928T>G