Canonical Allele Identifier: PA658681186
Gene: AP4M1 HGNC NCBI

Linked Data

ClinVar Variation Id: 450388
ClinVar RCV Id: RCV000519004 RCV000765978 RCV004017662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004713.2:p.Arg318Gln
CA4374881
NM_004722.4:c.953G>A