Canonical Allele Identifier: PA2826362767
Gene: AP4B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 402201
ClinVar RCV Id: RCV000454309 RCV001849375
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001240781.1:p.Phe319Leu
CA16609496
NM_001253852.3:c.955T>C
CA341712933
NM_001253852.3:c.957T>G
CA341712935
NM_001253852.3:c.957T>A