Canonical Allele Identifier: PA2742015181
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2759487
ClinVar RCV Id: RCV003498572
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Asp397Gly
CA391934489
NM_152594.3:c.1190A>G