Canonical Allele Identifier: PA2826163472
Gene: LRSAM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 365010
ClinVar RCV Id: RCV000649924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177652.1:p.Ala95Val
CA5246485
NM_001190723.3:c.284C>T