Canonical Allele Identifier: PA181089
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 177968
ClinVar RCV Id: RCV000154641 RCV000868561 RCV001133349 RCV001133350 RCV001133347 RCV001133348 RCV001134817 RCV001697052 RCV004534958
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser35071Cys
CA181087
NM_001267550.2:c.105212C>G