ClinGen Allele Registry
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Canonical Allele Identifier:
PA181683
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000154909
RCV000472564
RCV000617218
RCV000769915
RCV001133355
RCV001134826
RCV001134827
RCV001134828
RCV001134829
RCV001528765
RCV004544421
ClinVar Variation:
178182
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_596869.4:p.Arg25730Gln
CA181682
NM_133378.4:c.77189G>A