ClinGen Allele Registry
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Canonical Allele Identifier:
PA132856
Gene: TNNT2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000036595
RCV000225721
RCV000703215
RCV001798104
RCV002470731
RCV004018798
ClinVar Variation:
43647
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000355.2:p.Arg169Gln
CA004638
NM_000364.3:c.506G>A