Allele Registry

Canonical Allele Identifier: PA118737

Gene: SC5D HGNC NCBI

ClinVar RCV:

RCV000007780

ClinVar Variation:

7355

HGVS (amino-acid)	Matching Registered Transcripts
NP_008849.2:p.Gly211Asp	CA118736 NM_006918.5:c.632G>A