Canonical Allele Identifier: PA916065975
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg7324Cys
CA1994784
NM_133437.4:c.21970C>T