Canonical Allele Identifier: PA2829436757
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg13064His
CA237864
NM_003319.4:c.39191G>A