Canonical Allele Identifier: PA916065980
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191954

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ser7326Pro
CA237954
NM_133437.4:c.21976T>C