Allele Registry

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Canonical Allele Identifier: PA916005699

Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43633

ClinVar RCV Id: RCV000036580 RCV004017308

ClinVar Variation Id: 229336

ClinVar RCV Id: RCV000220636

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263274.1:p.His119Tyr	CA004375 NM_001276345.2:c.355C>T CA10576373 NM_001276345.2:c.354_355delinsGT