Canonical Allele Identifier: PA916065849
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 413130

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ile7175Thr
CA1994912
NM_133437.4:c.21524T>C