Canonical Allele Identifier: PA140397
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47229
ClinVar RCV Id: RCV000040499 RCV000241625 RCV000282835 RCV000337921 RCV000381175 RCV000341241 RCV000408381 RCV000466378 RCV001170583 RCV001703903 RCV004528213
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg20275Gln
CA140394
NM_001256850.1:c.60824G>A