ClinGen Allele Registry
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Canonical Allele Identifier:
PA916043908
Gene: AP4M1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
456182
ClinVar RCV:
RCV000549259
RCV001849402
ClinVar Variation:
471069
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001350600.1:p.Tyr291Ser
CA368472432
NM_001363671.2:c.872A>C