Allele Registry

Canonical Allele Identifier: PA2826200130

Gene: APTX HGNC NCBI

ClinVar RCV:

RCV000200146

RCV000357224

RCV001844083

RCV002517195

ClinVar Variation:

214126

HGVS (amino-acid)	Matching Registered Transcripts
NP_001182180.1:p.Trp6Cys	CA324705 NM_001195251.2:c.18G>T CA373181357 NM_001195251.2:c.18G>C