Canonical Allele Identifier: PA2830222598
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191861

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr20656Ser
CA237725
NM_133432.3:c.61967C>G
CA349524843
NM_133432.3:c.61966A>T