Canonical Allele Identifier: PA916043914
Gene: AP4M1 HGNC NCBI

Linked Data

ClinVar Variation Id: 383930
ClinVar RCV Id: RCV000422720 RCV001849370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350600.1:p.Cys326Tyr
CA16605611
NM_001363671.2:c.977G>A