Canonical Allele Identifier: PA2826163794
Gene: LRSAM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 365031
ClinVar RCV Id: RCV000527280 RCV002402086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177652.1:p.Ala564Val
CA5247123
NM_001190723.3:c.1691C>T