Canonical Allele Identifier: PA237955
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191954

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser13631Pro
CA237954
NM_133378.4:c.40891T>C