Canonical Allele Identifier: PA311950
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203294
ClinVar RCV Id: RCV000185387 RCV000713984 RCV001087209 RCV004537571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys7066Arg
CA311948
NM_001267550.2:c.21197A>G