Canonical Allele Identifier: PA2826177408
Gene: SAMD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 521232
ClinVar RCV Id: RCV000624410 RCV001281104
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180236.1:p.Glu974Lys
CA368189249
NM_001193307.1:c.2920G>A