Canonical Allele Identifier: PA099781
Gene: SEPTIN12 HGNC NCBI

Linked Data

ClinVar Variation Id: 37115
ClinVar RCV Id: RCV000030757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653206.2:p.Asp197Asn
CA130083
NM_144605.5:c.589G>A