Canonical Allele Identifier: PA2825345869
Gene: AP1G1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3127438
ClinVar RCV Id: RCV004424791

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025178.1:p.Pro206Ala
CA8156462
NM_001030007.2:c.616C>G