Allele Registry

Canonical Allele Identifier: PA2827416157

Gene: ERLIN1 HGNC NCBI

ClinVar RCV:

RCV000211706

ClinVar Variation:

226427

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334789.1:p.Gly50Val	CA10576346 NM_001347860.2:c.149G>T