Canonical Allele Identifier: PA289121
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 130688
ClinVar RCV Id: RCV000118797 RCV000317280 RCV000313328 RCV000355456 RCV001293103 RCV000273543 RCV000319315 RCV001082250 RCV000395255 RCV002444573 RCV001798370 RCV004542865
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Arg3113His
CA289115
NM_133379.5:c.9338G>A