Canonical Allele Identifier: PA2826163869
Gene: LRSAM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3019251
ClinVar RCV Id: RCV003871882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177652.1:p.Val643Met
CA5247223
NM_001190723.3:c.1927G>A