ClinGen Allele Registry
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Canonical Allele Identifier:
PA261456
Gene: TNNT2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000036576
RCV000159284
RCV000468546
RCV000619398
RCV001258056
RCV003450686
RCV003450687
RCV003450688
ClinVar Variation:
43629
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000355.2:p.Arg104Leu
CA004302
NM_000364.3:c.311G>T