Canonical Allele Identifier: PA645501314
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 393216
ClinVar RCV Id: RCV000421168
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006585.2:p.Pro77Leu
CA16603385
NM_006594.5:c.230C>T