Canonical Allele Identifier: PA2580524477
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1789831
ClinVar RCV Id: RCV002448266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Lys78Arg
CA391931935
NM_152594.3:c.233A>G