Canonical Allele Identifier: PA2742015194
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2817829
ClinVar RCV Id: RCV003601636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Cys436Ser
CA391934812
NM_152594.3:c.1306T>A
CA391934815
NM_152594.3:c.1307G>C