Canonical Allele Identifier: PA2830220142
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202875

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val16711Ala
CA310557
NM_133432.3:c.50132T>C