Canonical Allele Identifier: PA2573099366
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1341771
ClinVar RCV Id: RCV001837251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Asp11Val
CA391931859
NM_152594.3:c.32A>T