Canonical Allele Identifier: PA2828305258
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 366594
ClinVar RCV Id: RCV000390070 RCV001844151 RCV002523789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355933.1:p.Glu37Asp
CA10627234
NM_001369004.1:c.111A>T
CA373179788
NM_001369004.1:c.111A>C