Canonical Allele Identifier: PA2826410218
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179976

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys612Glu
CA185553
NM_001256850.1:c.1834A>G