Canonical Allele Identifier: PA2580347321
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2041494
ClinVar RCV Id: RCV002891136 RCV003375709
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006585.2:p.Leu274Phe
CA1016005
NM_006594.5:c.820C>T