Canonical Allele Identifier: PA2830208814
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238775
ClinVar RCV Id: RCV000231378
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val11397Gly
CA10581873
NM_133378.4:c.34190T>G