Canonical Allele Identifier: PA2828305191
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 4426
ClinVar RCV Id: RCV000004676

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355932.1:p.Pro118Leu
CA253142
NM_001369003.1:c.353C>T