Canonical Allele Identifier: PA645408802
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 290830
ClinVar RCV Id: RCV000387917 RCV000726557 RCV002328792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile4282Leu
CA2002660
NM_001267550.2:c.12844A>C