Canonical Allele Identifier: PA2828446530
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 559301
ClinVar RCV Id: RCV000676806 RCV002532176
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357598.1:p.Tyr95Cys
CA192400994
NM_001370669.1:c.284A>G