Canonical Allele Identifier: PA2742015158
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2740733
ClinVar RCV Id: RCV003497522
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Asp291Val
CA391933442
NM_152594.3:c.872A>T