Allele Registry

Canonical Allele Identifier: PA199574

Gene: SEPSECS HGNC NCBI

ClinVar RCV:

RCV000170363

RCV001565090

ClinVar Variation:

190145

HGVS (amino-acid)	Matching Registered Transcripts
NP_058651.3:p.Asp489Val	CA199573 NM_016955.3:c.1466A>T