ClinGen Allele Registry
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Canonical Allele Identifier:
PA261450
Gene: TNNT2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000036571
RCV000505760
RCV000556483
RCV000618563
RCV003450678
RCV003450679
RCV003450680
ClinVar Variation:
43626
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001001430.1:p.Asp86Ala
CA004228
NM_001001430.3:c.257A>C