Canonical Allele Identifier: PA2826422768
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser24664Cys
CA1989553
NM_001256850.1:c.73991C>G