Canonical Allele Identifier: PA141606
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47651
ClinVar RCV Id: RCV000040920 RCV001088345 RCV000786253 RCV002371852 RCV004534956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg3163Cys
CA141602
NM_001267550.2:c.9487C>T