Canonical Allele Identifier: PA645501056
Gene: TNXB HGNC NCBI

Linked Data

ClinVar Variation Id: 224352
ClinVar RCV Id: RCV000416571 RCV001564320
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115859.2:p.Arg600His
CA3732790
NM_032470.4:c.1799G>A