Canonical Allele Identifier: PA2829441793
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202973

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Pro21266Ser
CA310855
NM_003319.4:c.63796C>T