Allele Registry

Canonical Allele Identifier: PA123170

Gene: SELP HGNC NCBI

ClinVar RCV:

RCV000014482

RCV003964801

ClinVar Variation:

13527

HGVS (amino-acid)	Matching Registered Transcripts
NP_002996.2:p.Thr756Pro	CA123169 NM_003005.4:c.2266A>C