Canonical Allele Identifier: PA2830224918
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203043

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ser24047Pro
CA311067
NM_133432.3:c.72139T>C