Canonical Allele Identifier: PA2830201668
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1297569
ClinVar RCV Id: RCV001723337
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asn28078His
CA349495682
NM_133378.4:c.84232A>C