Canonical Allele Identifier: PA237621
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg31978Cys
CA237620
NM_133378.4:c.95932C>T