ClinGen Allele Registry
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Canonical Allele Identifier:
PA645387800
Gene: AP4M1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
369109
ClinVar RCV:
RCV000434728
RCV001088095
RCV003959945
ClinVar Variation:
386755
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_004713.2:p.Glu99Lys
CA4374557
NM_004722.4:c.295G>A