Canonical Allele Identifier: PA916064929
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46955
ClinVar RCV Id: RCV000040225 RCV000172337 RCV000294831 RCV000328437 RCV000343733 RCV000383259 RCV000399696 RCV000618332 RCV001079995 RCV002225277
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Val5237Ala
CA139618
NM_133437.4:c.15710T>C