Canonical Allele Identifier: PA645410033
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 377167
ClinVar RCV Id: RCV000441173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ile16683Asn
CA16603286
NM_001267550.2:c.50048T>A