Canonical Allele Identifier: PA184857
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 179657
ClinVar RCV Id: RCV000156453 RCV003531988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001430.1:p.Asn100Ser
CA004329
NM_001001430.3:c.299A>G