Canonical Allele Identifier: PA2580524469
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1978868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Asn10Asp
CA269282659
NM_152594.3:c.28A>G