Canonical Allele Identifier: PA2826163779
Gene: LRSAM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 472795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177652.1:p.Gln546Lys
CA5247113
NM_001190723.3:c.1636C>A