Canonical Allele Identifier: PA645412868
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405090
ClinVar RCV Id: RCV000461150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr35484Asn
CA16610278
NM_001267550.2:c.106451C>A