Canonical Allele Identifier: PA2825840486
Gene: SPART HGNC NCBI

Linked Data

ClinVar Variation Id: 424442
ClinVar RCV Id: RCV000483605
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135766.1:p.Ala23Asp
CA6949693
NM_001142294.2:c.68C>A