Canonical Allele Identifier: PA282658
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46582
ClinVar RCV Id: RCV000039852 RCV000251067 RCV000275658 RCV000301488 RCV000367878 RCV000333056 RCV000400937 RCV000993375 RCV001523697
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser3419Asn
CA282654
NM_001267550.2:c.10256G>A