Canonical Allele Identifier: PA2829436998
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 518646
ClinVar RCV Id: RCV000619118

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Val13423Ile
CA349423707
NM_003319.4:c.40267G>A