Canonical Allele Identifier: PA2825268786
Gene: LRSAM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 245886
ClinVar RCV Id: RCV001294857 RCV001705307 RCV002392727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005374.1:p.Ser505Leu
CA5247037
NM_001005374.4:c.1514C>T