Allele Registry

Canonical Allele Identifier: PA645394486

Gene: LRSAM1 HGNC NCBI

ClinVar Variation Id: 245886

HGVS (amino-acid)	Matching Registered Transcripts
NP_612370.3:p.Ser505Leu	CA5247037 NM_138361.5:c.1514C>T