Canonical Allele Identifier: PA2829441722
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Pro21166Ser
CA1987758
NM_003319.4:c.63496C>T