Canonical Allele Identifier: PA178625
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165907
ClinVar RCV Id: RCV000460153 RCV000152260 RCV002460047 RCV000724176
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg21155Cys
CA178623
NM_001267550.2:c.63463C>T