Canonical Allele Identifier: PA658664673
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466820
ClinVar RCV Id: RCV000542699 RCV000770102 RCV001722488 RCV004537979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr4668Ala
CA2002496
NM_001267550.2:c.14002A>G