Canonical Allele Identifier: PA2826933253
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 434226
ClinVar RCV Id: RCV000501595
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295241.1:p.Pro112Ser
CA1015999
NM_001308312.2:c.334C>T