Allele Registry

Canonical Allele Identifier: PA2826340672

Gene: SEL1L HGNC NCBI

ClinVar RCV:

RCV004123012

ClinVar Variation:

2268069

HGVS (amino-acid)	Matching Registered Transcripts
NP_001231913.1:p.Met186Val	CA7296174 NM_001244984.2:c.556A>G