ClinGen Allele Registry
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Canonical Allele Identifier:
PA139281
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000040090
RCV000415299
RCV000530713
RCV000730819
RCV000769897
RCV001134853
RCV001134854
RCV001134855
RCV001134856
RCV001134857
ClinVar Variation:
46820
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_596869.4:p.Arg8500Cys
CA139279
NM_133378.4:c.25498C>T