Canonical Allele Identifier: PA2829671072
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1393895
ClinVar RCV Id: RCV001898397 RCV004041499
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006585.2:p.Gly250Asp
CA1016019
NM_006594.5:c.749G>A