Canonical Allele Identifier: PA2826177244
Gene: SAMD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2120580
ClinVar RCV Id: RCV003059452
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180236.1:p.Arg708Lys
CA368192965
NM_001193307.1:c.2123G>A