ClinGen Allele Registry
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Canonical Allele Identifier:
PA916043929
Gene: AP4M1
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000192888
RCV000860999
RCV001507706
RCV001847852
RCV003895240
ClinVar Variation:
210207
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001350600.1:p.Ala455Thr
CA206016
NM_001363671.2:c.1363G>A