Allele Registry

Canonical Allele Identifier: PA100603

Gene: SEPSECS HGNC NCBI

ClinVar RCV:

RCV000000437

RCV001380417

RCV001582489

ClinVar Variation:

18401

HGVS (amino-acid)	Matching Registered Transcripts
NP_058651.3:p.Ala239Thr	CA114253 NM_016955.3:c.715G>A