Canonical Allele Identifier: PA916064946
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202625

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Met5272Thr
CA309793
NM_133437.4:c.15815T>C