Canonical Allele Identifier: PA2573092968
Gene: SAMD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1320287
ClinVar RCV Id: RCV001775460 RCV003120683 RCV003163910
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060124.2:p.Trp691Arg
CA4342896
NM_017654.4:c.2071T>C
CA368193400
NM_017654.4:c.2071T>A