Canonical Allele Identifier: PA2829442282
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467651
ClinVar RCV Id: RCV000591905 RCV001087664 RCV002367867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Pro22020Leu
CA1987332
NM_003319.4:c.66059C>T