Canonical Allele Identifier: PA2826412921
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 496946

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser5628Pro
CA2001734
NM_001256850.1:c.16882T>C