Canonical Allele Identifier: PA312011
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gln7163Pro
CA312010
NM_001256850.1:c.21488A>C