Canonical Allele Identifier: PA658665292
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467005
ClinVar RCV Id: RCV000537819 RCV001129105 RCV001129104 RCV001136087 RCV001136088 RCV001136089 RCV001584287 RCV001798883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile10549Val
CA1998891
NM_001267550.2:c.31645A>G