Canonical Allele Identifier: PA2573253277
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1469161
ClinVar RCV Id: RCV001972955

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006585.2:p.Glu448Lys
CA341710536
NM_006594.5:c.1342G>A