ClinGen Allele Registry
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Canonical Allele Identifier:
PA139523
Gene: TTN
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000040188
RCV000465574
RCV001170386
RCV001839596
RCV001839597
RCV001839598
RCV001839599
RCV002504909
RCV003137564
RCV004541150
ClinVar Variation:
46918
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_596869.4:p.Pro10595Thr
CA139521
NM_133378.4:c.31783C>A