Canonical Allele Identifier: PA916045172
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_001352205.1:p.Pro2949Thr
CA3733721
NM_001365276.2:c.8845C>A