ClinGen Allele Registry
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Canonical Allele Identifier:
PA181879
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000154973
RCV000287568
RCV000326198
RCV000327268
RCV000384268
RCV000387819
RCV000725482
RCV001084561
ClinVar Variation:
178236
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001254479.2:p.Arg7989Cys
CA181876
NM_001267550.2:c.23965C>T