Canonical Allele Identifier: PA2573304211
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1476804
ClinVar RCV Id: RCV001978126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Lys289Thr
CA7470194
NM_152594.3:c.866A>C