Canonical Allele Identifier: PA2573099365
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1309782
ClinVar RCV Id: RCV001756850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Thr5Arg
CA391931822
NM_152594.3:c.14C>G