Canonical Allele Identifier: PA2826163900
Gene: LRSAM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 408267
ClinVar RCV Id: RCV000468628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177652.1:p.Cys667Arg
CA5247259
NM_001190723.3:c.1999T>C