Canonical Allele Identifier: PA2826363038
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2554151
ClinVar RCV Id: RCV003304086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240782.1:p.Ile341Leu
CA28995389
NM_001253853.3:c.1021A>C