Allele Registry

Canonical Allele Identifier: PA2499300788

Gene: LSM11 HGNC NCBI

ClinVar RCV:

RCV001568350

ClinVar Variation:

1202617

HGVS (amino-acid)	Matching Registered Transcripts
NP_775762.1:p.Gly211Ser	CA361994750 NM_173491.4:c.631G>A