Canonical Allele Identifier: PA2573253278
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1480026
ClinVar RCV Id: RCV001991146
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006585.2:p.Ala453Ser
CA341710434
NM_006594.5:c.1357G>T