Canonical Allele Identifier: PA658680662
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467485
ClinVar RCV Id: RCV000537759 RCV000619486 RCV000714095 RCV001193720 RCV002476170 RCV001170103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Arg2540Cys
CA2004773
NM_133379.5:c.7618C>T