Canonical Allele Identifier: PA2825841077
Gene: SPART HGNC NCBI

Linked Data

ClinVar Variation Id: 216687

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135767.1:p.Asp391Gly
CA336976
NM_001142295.2:c.1172A>G