Allele Registry

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Canonical Allele Identifier: PA916005692

Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43625

ClinVar RCV Id: RCV000036570

ClinVar Variation Id: 666939

ClinVar RCV Id: RCV000825476

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263274.1:p.Asp98Glu	CA004247 NM_001276345.2:c.294T>G CA344206634 NM_001276345.2:c.294T>A