Canonical Allele Identifier: PA302498
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192001
ClinVar RCV Id: RCV000172373 RCV000412691 RCV001130093 RCV001130094 RCV001130095 RCV001130801 RCV001130800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg9489Trp
CA302495
NM_001267550.2:c.28465C>T