Allele Registry

Canonical Allele Identifier: PA2580321601

Gene: SEL1L HGNC NCBI

ClinVar RCV:

RCV004123012

ClinVar Variation:

2268069

HGVS (amino-acid)	Matching Registered Transcripts
NP_005056.3:p.Met186Val	CA7296174 NM_005065.6:c.556A>G