Canonical Allele Identifier: PA916066055
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238790

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg7466Trp
CA1994704
NM_133437.4:c.22396C>T