Canonical Allele Identifier: PA2828446515
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 366594
ClinVar RCV Id: RCV000390070 RCV001844151 RCV002523789
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357598.1:p.Glu37Asp
CA10627234
NM_001370669.1:c.111A>T
CA373179788
NM_001370669.1:c.111A>C