ClinGen Allele Registry
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Canonical Allele Identifier:
PA261447
Gene: TNNT2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000036562
RCV000553495
RCV001179840
RCV001253102
RCV002426557
ClinVar Variation:
43618
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000355.2:p.Asn83Ser
CA088088
NM_000364.3:c.248A>G