Canonical Allele Identifier: PA916043895
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_001350600.1:p.Glu118Asp
CA209697
NM_001363671.2:c.354A>C
CA368466570
NM_001363671.2:c.354A>T