ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826554774
Gene: TNNT2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
43636
ClinVar RCV Id:
RCV000036583
RCV000159290
RCV000243733
RCV000468121
RCV001187129
RCV002470730
RCV003450693
RCV003450694
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263275.1:p.Arg100Cys
CA004443
NM_001276346.2:c.298C>T