Canonical Allele Identifier: PA645501313
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 240688
ClinVar RCV Id: RCV000226405 RCV002429124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006585.2:p.Cys73Ser
CA1016161
NM_006594.5:c.217T>A
CA341691515
NM_006594.5:c.218G>C