Canonical Allele Identifier: PA2830204061
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro32296Leu
CA1985394
NM_133378.4:c.96887C>T