Canonical Allele Identifier: PA2742015024
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2761345
ClinVar RCV Id: RCV003498620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Gly35Glu
CA391934076
NM_152594.3:c.104G>A