Canonical Allele Identifier: PA2830210571
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Val1156Ala
CA179349
NM_133432.3:c.3467T>C