Canonical Allele Identifier: PA2573099386
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1334214
ClinVar RCV Id: RCV001813629 RCV003163948
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Ala409Val
CA7470252
NM_152594.3:c.1226C>T