Canonical Allele Identifier: PA1139762641
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 970869
ClinVar RCV Id: RCV001246524
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Asn10Ser
CA391931851
NM_152594.3:c.29A>G