ClinGen Allele Registry
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Canonical Allele Identifier:
PA916005782
Gene: TNNT2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000119344
RCV000612990
RCV000646060
RCV000777699
RCV001781461
RCV002055314
RCV002055315
ClinVar Variation:
132943
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263274.1:p.Arg154Trp
CA004554
NM_001276345.2:c.460C>T