Canonical Allele Identifier: PA2825268050
Gene: LRSAM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 380607
ClinVar RCV Id: RCV000863528 RCV001174252 RCV002266963
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005373.1:p.Thr534Met
CA5247076
NM_001005373.4:c.1601C>T