ClinGen Allele Registry
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Canonical Allele Identifier:
PA1139698107
Gene: TNNT2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000036607
RCV000211868
RCV000223828
RCV000247384
RCV000524543
RCV001798105
RCV002051803
RCV003450713
ClinVar Variation:
43659
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263274.1:p.Lys220del
CA006429
NM_001276345.2:c.659_661del