Canonical Allele Identifier: PA645394492
Gene: LRSAM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 365031

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_612370.3:p.Ala591Val
CA5247123
NM_138361.5:c.1772C>T