ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825225832
Gene: TNNT2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000013222
RCV000036622
RCV000148898
RCV000157540
RCV000159322
RCV000162331
RCV000203739
RCV000248304
RCV000755702
RCV000768493
RCV000771167
ClinVar Variation:
12411
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001001432.1:p.Arg272Cys
CA005245
NM_001001432.3:c.814C>T