Canonical Allele Identifier: PA150965
Gene: TCTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 126288
ClinVar RCV Id: RCV000114230 RCV000204827 RCV000625192 RCV001110871 RCV003390794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079085.2:p.Arg200Gln
CA150964
NM_024809.5:c.599G>A