Canonical Allele Identifier: PA2830209206
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203097

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr32593Asn
CA311229
NM_133378.4:c.97778C>A