Canonical Allele Identifier: PA2826426146
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405081

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg30206Cys
CA1986938
NM_001256850.1:c.90616C>T