Canonical Allele Identifier: PA645450918
Gene: TNXB HGNC NCBI

Linked Data

ClinVar Variation Id: 261172
ClinVar RCV Id: RCV000243088 RCV002278206 RCV001660340 RCV002374424
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061978.6:p.Pro2947Thr
CA3733721
NM_019105.8:c.8839C>A