Canonical Allele Identifier: PA2830227234
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1197339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr26510Ser
CA1985126
NM_133432.3:c.79529C>G
CA349405967
NM_133432.3:c.79528A>T