Allele Registry

Canonical Allele Identifier: PA2741896716

Gene: SELP HGNC NCBI

ClinVar RCV:

RCV003977419

ClinVar Variation:

3060479

HGVS (amino-acid)	Matching Registered Transcripts
NP_002996.2:p.Ser331Asn	CA1235275 NM_003005.4:c.992G>A