Canonical Allele Identifier: PA916043915
Gene: AP4M1 HGNC NCBI

Linked Data

ClinVar Variation Id: 210216
ClinVar RCV Id: RCV000193207 RCV001040211 RCV001849338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350600.1:p.Cys326Arg
CA206534
NM_001363671.2:c.976T>C