Canonical Allele Identifier: PA1139686422
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 859557
ClinVar RCV Id: RCV001065696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240782.1:p.Arg14Gly
CA341689077
NM_001253853.3:c.40A>G