Canonical Allele Identifier: PA658813448
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser9384Cys
CA1999652
NM_001267550.2:c.28151C>G