Allele Registry

Canonical Allele Identifier: PA204769

Gene: LRSAM1 HGNC NCBI

ClinVar RCV:

RCV000190742

RCV001173632

RCV001224770

ClinVar Variation:

208726

HGVS (amino-acid)	Matching Registered Transcripts
NP_612370.3:p.Pro707Leu	CA204767 NM_138361.5:c.2120C>T