Canonical Allele Identifier: PA2580524528
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1743455
ClinVar RCV Id: RCV002338100
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Ser396Gly
CA7470238
NM_152594.3:c.1186A>G