Canonical Allele Identifier: PA140389
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47222
ClinVar RCV Id: RCV000040492 RCV000172648 RCV000285866 RCV000289204 RCV000341054 RCV000325515 RCV000383806 RCV000617230 RCV001084400 RCV001170804 RCV004534919
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr21820Ile
CA140385
NM_001267550.2:c.65459C>T