Canonical Allele Identifier: PA2830196157
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202702
ClinVar RCV Id: RCV000308035 RCV000339816 RCV000394227 RCV000474495 RCV000361668 RCV000394317 RCV001262302 RCV001798650 RCV001532426 RCV003114341 RCV002426896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile15000Val
CA310028
NM_133378.4:c.44998A>G