Canonical Allele Identifier: PA2828305091
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 2321145
ClinVar RCV Id: RCV002893652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355931.1:p.Val100Leu
CA373177766
NM_001369002.1:c.298G>C
CA373177768
NM_001369002.1:c.298G>T