Canonical Allele Identifier: PA2825840814
Gene: SPART HGNC NCBI

Linked Data

ClinVar Variation Id: 311764
ClinVar RCV Id: RCV000279728 RCV001850648 RCV004021570
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135766.1:p.Asp652Asn
CA6949246
NM_001142294.2:c.1954G>A