Canonical Allele Identifier: PA181531
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 178134
ClinVar RCV Id: RCV000154849 RCV000456632 RCV000586323 RCV001813401 RCV004019853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Val309Ala
CA181530
NM_152594.3:c.926T>C