Canonical Allele Identifier: PA2826200297
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 214121
ClinVar RCV Id: RCV000195599 RCV003765258
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182181.2:p.Arg173His
CA319960
NM_001195252.2:c.518G>A