Canonical Allele Identifier: PA645412517
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332708

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg33104Cys
CA1986202
NM_001267550.2:c.99310C>T