Canonical Allele Identifier: PA2825840637
Gene: SPART HGNC NCBI

Linked Data

ClinVar Variation Id: 461200

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135766.1:p.Lys377Met
CA6949485
NM_001142294.2:c.1130A>T