Canonical Allele Identifier: PA209698
Gene: AP4M1 HGNC NCBI

Linked Data

ClinVar Variation Id: 210212
ClinVar RCV Id: RCV000195099 RCV000766902 RCV001087871 RCV003927759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004713.2:p.Glu111Asp
CA209697
NM_004722.4:c.333A>C
CA368466570
NM_004722.4:c.333A>T