Allele Registry

Canonical Allele Identifier: PA645394490

Gene: LRSAM1 HGNC NCBI

ClinVar Variation Id: 380607

HGVS (amino-acid)	Matching Registered Transcripts
NP_612370.3:p.Thr534Met	CA5247076 NM_138361.5:c.1601C>T