Canonical Allele Identifier: PA916043900
Gene: AP4M1 HGNC NCBI

Linked Data

ClinVar Variation Id: 30264
ClinVar RCV Id: RCV000023191 RCV001849279 RCV002272028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350600.1:p.Glu200Lys
CA342728
NM_001363671.2:c.598G>A