Canonical Allele Identifier: PA112645
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 12654
ClinVar RCV Id: RCV000013490 RCV001319595
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile34306Asn
CA341213
NM_001256850.1:c.102917T>A