Canonical Allele Identifier: PA2742015156
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2986269
ClinVar RCV Id: RCV003843940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Lys289Asn
CA391933430
NM_152594.3:c.867A>C
CA391933431
NM_152594.3:c.867A>T