Canonical Allele Identifier: PA2828304293
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 559301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355924.1:p.Tyr183Cys
CA192400994
NM_001368995.1:c.548A>G