Canonical Allele Identifier: PA2829900954
Gene: TNXB HGNC NCBI

Linked Data

ClinVar Variation Id: 224352
ClinVar RCV Id: RCV000416571 RCV001564320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061978.6:p.Arg4169His
CA3732790
NM_019105.8:c.12506G>A