ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826555003
Gene: TNNT2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000172136
RCV000466482
RCV000620239
RCV000986502
RCV001177367
RCV003453242
RCV003453243
ClinVar Variation:
181630
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263275.1:p.Asp216Asn
CA005066
NM_001276346.2:c.646G>A