Canonical Allele Identifier: PA2826200197
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 4426
ClinVar RCV Id: RCV000004676

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182180.1:p.Pro206Leu
CA253142
NM_001195251.2:c.617C>T