Canonical Allele Identifier: PA237763
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191876
ClinVar RCV Id: RCV000172233 RCV000295809 RCV000328290 RCV000332094 RCV000372796 RCV000387397 RCV001086678 RCV002345590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg27563His
CA237761
NM_001267550.2:c.82688G>A