Canonical Allele Identifier: PA645501316
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 390620
ClinVar RCV Id: RCV000436086
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006585.2:p.Ala216Gly
CA16603384
NM_006594.5:c.647C>G