Canonical Allele Identifier: PA2828305020
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 1807152
ClinVar RCV Id: RCV002475109
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355930.1:p.Gly186Val
CA373176969
NM_001369001.1:c.557G>T