Canonical Allele Identifier: PA916066716
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404849

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Leu9008Val
CA1993760
NM_133437.4:c.27022C>G