Canonical Allele Identifier: PA658806757
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 499609
ClinVar RCV Id: RCV000597141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Ile3528Thr
CA349667579
NM_133379.5:c.10583T>C