Canonical Allele Identifier: PA2826362959
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2048203
ClinVar RCV Id: RCV002918622
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240782.1:p.Gln127His
CA341713913
NM_001253853.3:c.381A>C
CA341713915
NM_001253853.3:c.381A>T