Canonical Allele Identifier: PA645410632
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332806
ClinVar RCV Id: RCV000273244 RCV000310901 RCV000325941 RCV000365624 RCV000404582 RCV000643671 RCV002365396 RCV003335308
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Trp21804Arg
CA1991706
NM_001267550.2:c.65410T>C
CA349434242
NM_001267550.2:c.65410T>A