Canonical Allele Identifier: PA2826887493
Gene: SAMD9L HGNC NCBI

Linked Data

ClinVar Variation Id: 446530
ClinVar RCV Id: RCV000515805 RCV001270308 RCV001557094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290429.1:p.Arg986Cys
CA368185911
NM_001303500.3:c.2956C>T