Canonical Allele Identifier: PA645381978
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332971
ClinVar RCV Id: RCV000279118 RCV000287427 RCV000342328 RCV000373662 RCV000399983 RCV000476774 RCV001729544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Thr206Lys
CA2006274
NM_133379.5:c.617C>A