Canonical Allele Identifier: PA2830232467
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238802

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Asn10007Lys
CA1993218
NM_133437.4:c.30021C>A
CA349528489
NM_133437.4:c.30021C>G