Canonical Allele Identifier: PA2828304432
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 2230216
ClinVar RCV Id: RCV002717498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355925.1:p.Ser212Ile
CA373177338
NM_001368996.1:c.635G>T