Canonical Allele Identifier: PA2830216665
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467325
ClinVar RCV Id: RCV000545524

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg10840Ser
CA349494156
NM_133432.3:c.32520G>T
CA349494157
NM_133432.3:c.32520G>C