Canonical Allele Identifier: PA658817386
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 539528
ClinVar RCV Id: RCV000649279 RCV002311984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006585.2:p.Val300Leu
CA1015986
NM_006594.5:c.898G>T
CA341713165
NM_006594.5:c.898G>C