Canonical Allele Identifier: PA206017
Gene: AP4M1 HGNC NCBI

Linked Data

ClinVar Variation Id: 210207
ClinVar RCV Id: RCV000192888 RCV000860999 RCV001507706 RCV001847852 RCV003895240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004713.2:p.Ala448Thr
CA206016
NM_004722.4:c.1342G>A