Canonical Allele Identifier: PA2830203814
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404971

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg32042Cys
CA1985539
NM_133378.4:c.96124C>T