Canonical Allele Identifier: PA2830232662
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202731
ClinVar RCV Id: RCV000313228 RCV000352827 RCV000356258 RCV000396308 RCV000228391 RCV000398470 RCV000714055 RCV000764322 RCV001170369 RCV003235108 RCV002444755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Tyr10346Phe
CA310113
NM_133437.4:c.31037A>T