Canonical Allele Identifier: PA2580177009
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2112120
ClinVar RCV Id: RCV003034387

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gln34806Pro
CA349411780
NM_001267550.2:c.104417A>C