Canonical Allele Identifier: PA916066238
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166007

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg7954Gln
CA178820
NM_133437.4:c.23861G>A