Canonical Allele Identifier: PA2830225755
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405075

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Trp25132Arg
CA1985790
NM_133432.3:c.75394T>C
CA349418116
NM_133432.3:c.75394T>A