Canonical Allele Identifier: PA658816836
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala31784Val
CA349462688
NM_001267550.2:c.95351C>T