Canonical Allele Identifier: PA1139762633
Gene: SPRED1 HGNC NCBI

Linked Data

ClinVar Variation Id: 965391

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689807.1:p.Ser2Arg
CA391931794
NM_152594.3:c.4A>C
CA391931800
NM_152594.3:c.6C>A
CA391931801
NM_152594.3:c.6C>G