Canonical Allele Identifier: PA2828102330
Gene: AP4M1 HGNC NCBI

Linked Data

ClinVar Variation Id: 471065
ClinVar RCV Id: RCV000529550 RCV003278904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350600.1:p.Asp43Glu
CA4374445
NM_001363671.2:c.129C>A
CA368463885
NM_001363671.2:c.129C>G