Canonical Allele Identifier: PA645412812
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332686
ClinVar RCV Id: RCV000273903 RCV000298551 RCV000313614 RCV000355738 RCV000396822 RCV000607925 RCV003137936
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg35136Trp
CA1985267
NM_001267550.2:c.105406C>T