Canonical Allele Identifier: PA2830209363
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2943577
ClinVar RCV Id: RCV003803135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Tyr32898Cys
CA349405532
NM_133378.4:c.98693A>G