Canonical Allele Identifier: PA2830214473
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202659

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ser7006Pro
CA309899
NM_133432.3:c.21016T>C