Canonical Allele Identifier: PA2826421408
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238834

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile22078Val
CA1990671
NM_001256850.1:c.66232A>G