Canonical Allele Identifier: PA2828446623
Gene: APTX HGNC NCBI

Linked Data

ClinVar Variation Id: 290957
ClinVar RCV Id: RCV000324352
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357598.1:p.Pro242His
CA10606959
NM_001370669.1:c.725C>A