ClinGen Allele Registry
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Canonical Allele Identifier:
PA113483
Gene: TNNT2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000154216
RCV000471745
RCV000617860
RCV001004907
RCV003453149
RCV003453150
ClinVar Variation:
177634
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263274.1:p.Ser189Phe
CA004746
NM_001276345.2:c.566C>T