Canonical Allele Identifier: PA2826163865
Gene: LRSAM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 948931
ClinVar RCV Id: RCV001220288

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177652.1:p.Pro638Ala
CA5247222
NM_001190723.3:c.1912C>G