Canonical Allele Identifier: PA645387909
Gene: AP4M1 HGNC NCBI

Linked Data

ClinVar Variation Id: 386884
ClinVar RCV Id: RCV000433329 RCV000765979 RCV001849371 RCV001848781
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004713.2:p.Arg367Gln
CA4374971
NM_004722.4:c.1100G>A