Canonical Allele Identifier: PA2580179933
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1927981
ClinVar RCV Id: RCV002621980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240782.1:p.Ser9Ile
CA341689248
NM_001253853.3:c.26G>T