Canonical Allele Identifier: PA2830214371
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238787
ClinVar RCV Id: RCV000231819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Thr6826Ser
CA10581867
NM_133432.3:c.20476A>T
CA349618178
NM_133432.3:c.20477C>G