Canonical Allele Identifier: PA916065764
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Val7041Leu
CA1994994
NM_133437.4:c.21121G>C