Canonical Allele Identifier: PA2573304227
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1490638
ClinVar RCV Id: RCV001978630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Arg403Gln
CA7470245
NM_152594.3:c.1208G>A