Allele Registry

Canonical Allele Identifier: PA250032

Gene: TBX19 HGNC NCBI

ClinVar RCV:

RCV000005775

ClinVar Variation:

5442

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