Canonical Allele Identifier: PA658817371
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 516957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly35376Ala
CA1985162
NM_001267550.2:c.106127G>C