Canonical Allele Identifier: PA916043923
Gene: AP4M1 HGNC NCBI

Linked Data

ClinVar Variation Id: 522649
ClinVar RCV Id: RCV000625788
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350600.1:p.Phe416Leu
CA4375034
NM_001363671.2:c.1246T>C
CA368476862
NM_001363671.2:c.1248C>A
CA368476878
NM_001363671.2:c.1248C>G