Canonical Allele Identifier: PA1139762816
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 981597
ClinVar RCV Id: RCV001261133 RCV001880008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Ser279Asn
CA269293447
NM_152594.3:c.836G>A