Canonical Allele Identifier: PA2828304999
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 2321145
ClinVar RCV Id: RCV002893652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355930.1:p.Val134Leu
CA373177766
NM_001369001.1:c.400G>C
CA373177768
NM_001369001.1:c.400G>T