Canonical Allele Identifier: PA1139762643
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 966373
ClinVar RCV Id: RCV001241033
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Asp11Asn
CA391931854
NM_152594.3:c.31G>A