Canonical Allele Identifier: PA283812
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47367
ClinVar RCV Id: RCV000040637 RCV000252077 RCV000338511 RCV000299007 RCV000311963 RCV000369992 RCV000399563 RCV000993488 RCV001514400
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile26225Thr
CA283808
NM_001267550.2:c.78674T>C