Canonical Allele Identifier: PA2830207804
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404954
ClinVar RCV Id: RCV000472229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr30604Asn
CA16610290
NM_133378.4:c.91811C>A