Canonical Allele Identifier: PA658817056
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 518891
ClinVar RCV Id: RCV000617377 RCV000643506 RCV001562342
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile33353Thr
CA1986083
NM_001267550.2:c.100058T>C