Canonical Allele Identifier: PA2829433236
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202659

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ser6881Pro
CA309899
NM_003319.4:c.20641T>C