ClinGen Allele Registry
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Canonical Allele Identifier:
PA113449
Gene: TNNT2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000013217
RCV000013218
RCV000013219
RCV000159272
RCV000211864
RCV000243910
RCV000684789
RCV001171170
ClinVar Variation:
12408
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263274.1:p.Ile89Asn
CA004157
NM_001276345.2:c.266T>A