Canonical Allele Identifier: PA2830193172
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 413123
ClinVar RCV Id: RCV000473976 RCV001134655 RCV001134654 RCV001133195 RCV001133196 RCV001133197 RCV001562414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp7008Glu
CA2000366
NM_133378.4:c.21024T>G
CA349496831
NM_133378.4:c.21024T>A