Canonical Allele Identifier: PA2826428892
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 262342

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala33605Gly
CA1985217
NM_001256850.1:c.100814C>G