Canonical Allele Identifier: PA916043913
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_001350600.1:p.Arg325Gln
CA4374881
NM_001363671.2:c.974G>A