Allele Registry

Canonical Allele Identifier: PA100614

Gene: SEPSECS HGNC NCBI

ClinVar RCV:

RCV000000436

RCV001380416

ClinVar Variation:

18400

HGVS (amino-acid)	Matching Registered Transcripts
NP_058651.3:p.Tyr334Cys	CA114252 NM_016955.3:c.1001A>G