Canonical Allele Identifier: PA2830379856
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 2230216
ClinVar RCV Id: RCV002717498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_778243.1:p.Ser212Ile
CA373177338
NM_175073.3:c.635G>T