Canonical Allele Identifier: PA336978
Gene: SPART HGNC NCBI

Linked Data

ClinVar Variation Id: 216687
ClinVar RCV Id: RCV000197093 RCV000713445 RCV001847900 RCV003278697 RCV001640302 RCV003907749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055902.1:p.Asp391Gly
CA336976
NM_015087.5:c.1172A>G