Canonical Allele Identifier: PA2830318356
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3229271
ClinVar RCV Id: RCV004524850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Ser287Asn
CA391933413
NM_152594.3:c.860G>A