Canonical Allele Identifier: PA645501319
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 386852

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006585.2:p.Val252Ala
CA1016017
NM_006594.5:c.755T>C