Canonical Allele Identifier: PA2826427697
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191822

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg32451His
CA237632
NM_001256850.1:c.97352G>A