Canonical Allele Identifier: PA181620
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96315

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg29787His
CA181617
NM_001256850.1:c.89360G>A