Canonical Allele Identifier: PA2573304221
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1362601
ClinVar RCV Id: RCV001934499
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Phe342Tyr
CA391933821
NM_152594.3:c.1025T>A