Canonical Allele Identifier: PA142275
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 47967
ClinVar RCV Id: RCV000041240 RCV000680360 RCV001813368 RCV001082112 RCV002453336 RCV003944953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Asp9Val
CA142274
NM_152594.3:c.26A>T