Canonical Allele Identifier: PA915979699
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 663108
ClinVar RCV Id: RCV000820911 RCV001849123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006585.2:p.Leu499Phe
CA1015783
NM_006594.5:c.1497G>T
CA341709750
NM_006594.5:c.1497G>C