ClinGen Allele Registry
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Canonical Allele Identifier:
PA916006036
Gene: TNNT2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000036624
RCV000148900
RCV000149450
RCV000588568
RCV000755701
RCV000771256
RCV000852592
RCV001081698
RCV001099310
RCV001099311
RCV002433498
ClinVar Variation:
43675
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263275.1:p.Ala38Val
CA004079
NM_001276346.2:c.113C>T