Canonical Allele Identifier: PA2826163855
Gene: LRSAM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1506530
ClinVar RCV Id: RCV002006799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177652.1:p.Pro628Leu
CA5247215
NM_001190723.3:c.1883C>T