Canonical Allele Identifier: PA2826933271
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 402201
ClinVar RCV Id: RCV000454309 RCV001849375
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295241.1:p.Phe151Leu
CA16609496
NM_001308312.2:c.451T>C
CA341712933
NM_001308312.2:c.453T>G
CA341712935
NM_001308312.2:c.453T>A