Canonical Allele Identifier: PA2830221421
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47421
ClinVar RCV Id: RCV000040691 RCV000172628 RCV000252102 RCV001130325 RCV001130327 RCV001130324 RCV001130326 RCV000476606 RCV001130323 RCV001170783
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val18784Gly
CA140941
NM_133432.3:c.56351T>G