Canonical Allele Identifier: PA658681182
Gene: AP4M1 HGNC NCBI

Linked Data

ClinVar Variation Id: 471069
ClinVar RCV Id: RCV000549259 RCV001849402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004713.2:p.Tyr284Ser
CA368472432
NM_004722.4:c.851A>C