Canonical Allele Identifier: PA141452
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47589
ClinVar RCV Id: RCV000040858 RCV000172611 RCV000248871 RCV000282930 RCV000291082 RCV000322814 RCV000379720 RCV000383122 RCV000769863 RCV001086482 RCV001293119
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg32587Pro
CA141448
NM_001267550.2:c.97760G>C