Canonical Allele Identifier: PA2828304906
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 4426
ClinVar RCV Id: RCV000004676

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355929.1:p.Pro152Leu
CA253142
NM_001369000.1:c.455C>T