Canonical Allele Identifier: PA658817201
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497011

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg34596His
CA1985541
NM_001267550.2:c.103787G>A