Canonical Allele Identifier: PA2829439938
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47409
ClinVar RCV Id: RCV000040679 RCV000265407 RCV000300600 RCV000304128 RCV000361272 RCV000391590 RCV000726237 RCV002345317
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ile18342Thr
CA140918
NM_003319.4:c.55025T>C