Canonical Allele Identifier: PA2826362954
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 390620
ClinVar RCV Id: RCV000436086
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240782.1:p.Ala117Gly
CA16603384
NM_001253853.3:c.350C>G