Canonical Allele Identifier: PA2826425889
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467665
ClinVar RCV Id: RCV000534410

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg29879Lys
CA60972642
NM_001256850.1:c.89636G>A