Canonical Allele Identifier: PA2830209077
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 945244
ClinVar RCV Id: RCV001215836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Tyr32218Cys
CA349411918
NM_133378.4:c.96653A>G