Canonical Allele Identifier: PA2825225022
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43648
ClinVar RCV Id: RCV000211867 RCV000459834 RCV000620577 RCV000624557 RCV002286700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001432.1:p.Glu158del
CA004651
NM_001001432.3:c.472_474del
CA077423
NM_001001432.3:c.469G>T
CA344204544
NM_001001432.3:c.472G>T
CA344204579
NM_001001432.3:c.466G>T
CA344204597
NM_001001432.3:c.463G>T