Canonical Allele Identifier: PA658664719
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 468802
ClinVar RCV Id: RCV000532253
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Arg325Gln
CA391933663
NM_152594.3:c.974G>A