Canonical Allele Identifier: PA2830227262
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47705
ClinVar RCV Id: RCV000040974
ClinVar Variation Id: 1394513
ClinVar RCV Id: RCV001884827
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr26542Ser
CA141748
NM_133432.3:c.79625C>G
CA349405236
NM_133432.3:c.79624A>T