Canonical Allele Identifier: PA302786
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 194910
ClinVar RCV Id: RCV000219227 RCV000618077 RCV000724241 RCV001079420 RCV000769015 RCV004537383
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg12125Cys
CA302785
NM_133378.4:c.36373C>T