Canonical Allele Identifier: PA2826177253
Gene: SAMD9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2818324
ClinVar RCV Id: RCV003713661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180236.1:p.Met717del
CA2739278680
NM_001193307.1:c.2148_2150del