Canonical Allele Identifier: PA302908
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196082

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val21725Ala
CA302906
NM_001256850.1:c.65174T>C