Canonical Allele Identifier: PA658681174
Gene: AP4M1 HGNC NCBI

Linked Data

ClinVar Variation Id: 471065
ClinVar RCV Id: RCV000529550 RCV003278904
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004713.2:p.Asp43Glu
CA4374445
NM_004722.4:c.129C>A
CA368463885
NM_004722.4:c.129C>G