Canonical Allele Identifier: PA2742014995
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2828445
ClinVar RCV Id: RCV003601826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Asp9Asn
CA391931844
NM_152594.3:c.25G>A