Canonical Allele Identifier: PA916066000
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Pro7370Thr
CA1994759
NM_133437.4:c.22108C>A