Canonical Allele Identifier: PA2830232996
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467325
ClinVar RCV Id: RCV000545524

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg10907Ser
CA349494156
NM_133437.4:c.32721G>T
CA349494157
NM_133437.4:c.32721G>C