Canonical Allele Identifier: PA2828446737
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 214121
ClinVar RCV Id: RCV000195599 RCV003765258
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357599.1:p.Arg157His
CA319960
NM_001370670.1:c.470G>A