ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2829435706
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar Variation Id:
165924
ClinVar RCV Id:
RCV000152268
RCV000461956
RCV000618661
RCV001085555
RCV001132664
RCV001171295
RCV001132661
RCV001132662
RCV001132663
RCV001136052
RCV004532694
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_003310.4:p.Leu11315Met
CA211117
NM_003319.4:c.33943C>A