Canonical Allele Identifier: PA2573067871
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1310614
ClinVar RCV Id: RCV001767728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240782.1:p.Arg8Gly
CA1016139
NM_001253853.3:c.22C>G