Canonical Allele Identifier: PA237762
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191876
ClinVar RCV Id: RCV000172233 RCV000295809 RCV000328290 RCV000332094 RCV000372796 RCV000387397 RCV001086678 RCV002345590
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg24995His
CA237761
NM_133378.4:c.74984G>A