Canonical Allele Identifier: PA140970
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47430
ClinVar RCV Id: RCV000040699 RCV000293712 RCV000336932 RCV000375171 RCV000335686 RCV000392066 RCV000475754 RCV000727431 RCV000852498 RCV002345323
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg25389Thr
CA140968
NM_133378.4:c.76166G>C