Canonical Allele Identifier: PA2830240586
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191843
ClinVar RCV Id: RCV000172184

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asp23140His
CA237680
NM_133437.4:c.69418G>C