Canonical Allele Identifier: PA2580334930
Gene: SC5D HGNC NCBI

Linked Data

ClinVar Variation Id: 2071013
ClinVar RCV Id: RCV002971589

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008849.2:p.Asp237Glu
CA6328221
NM_006918.5:c.711C>G
CA383030444
NM_006918.5:c.711C>A