Canonical Allele Identifier: PA2829445654
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Thr26096Asn
CA311229
NM_003319.4:c.78287C>A