Allele Registry

Canonical Allele Identifier: PA2499285529

Gene: TNXB HGNC NCBI

ClinVar RCV:

RCV001561078

RCV002414267

RCV002495895

ClinVar Variation:

1197303

HGVS (amino-acid)	Matching Registered Transcripts
NP_061978.6:p.Pro2601Leu	CA3734051 NM_019105.8:c.7802C>T