Canonical Allele Identifier: PA2826363040
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1174650
ClinVar RCV Id: RCV001528332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240782.1:p.Gly345Val
CA341710572
NM_001253853.3:c.1034G>T