Allele Registry

Canonical Allele Identifier: PA2828174701

Gene: TNXB HGNC NCBI

ClinVar RCV:

RCV001561078

RCV002414267

RCV002495895

ClinVar Variation:

1197303

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352205.1:p.Pro2601Leu	CA3734051 NM_001365276.2:c.7802C>T