Canonical Allele Identifier: PA105921
Gene: TUBB2B HGNC NCBI

Linked Data

ClinVar Variation Id: 428
ClinVar RCV Id: RCV000000456
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_821080.1:p.Phe265Leu
CA250426
NM_178012.5:c.793T>C
CA362586891
NM_178012.5:c.795C>A
CA362586893
NM_178012.5:c.795C>G