Canonical Allele Identifier: PA250032
Gene: TBX19 HGNC NCBI

Linked Data

ClinVar Variation Id: 5442
ClinVar RCV Id: RCV000005775
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005140.1:p.Met86Arg
CA250031
NM_005149.2:c.257T>G