Canonical Allele Identifier: PA100798
Gene: SEPTIN9 HGNC NCBI

Linked Data

ClinVar Variation Id: 5863
ClinVar RCV Id: RCV000006221 RCV000516514 RCV004018574
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001106963.1:p.Arg106Trp
CA340468
NM_001113491.2:c.316C>T