Canonical Allele Identifier: PA2828175801
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_001352205.1:p.Arg4171His
CA3732790
NM_001365276.2:c.12512G>A