Canonical Allele Identifier: PA2826200371
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 366594

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182183.1:p.Glu71Asp
CA10627234
NM_001195254.2:c.213A>T
CA373179788
NM_001195254.2:c.213A>C