Canonical Allele Identifier: PA179279
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166310
ClinVar RCV Id: RCV000152495 RCV000229239 RCV000185187 RCV001293099 RCV001798486 RCV002372004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg2354Cys
CA179276
NM_001267550.2:c.7060C>T