Canonical Allele Identifier: PA139282
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46820
ClinVar RCV Id: RCV000040090 RCV000415299 RCV000530713 RCV000730819 RCV000769897 RCV001134854 RCV001134856 RCV001134853 RCV001134855 RCV001134857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg9744Cys
CA139279
NM_001267550.2:c.29230C>T