Canonical Allele Identifier: PA2830193489
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238729
ClinVar RCV Id: RCV000230408 RCV000594931 RCV000727265
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asn7822Lys
CA1999851
NM_133378.4:c.23466C>G
CA349456157
NM_133378.4:c.23466C>A