Canonical Allele Identifier: PA141681
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47673
ClinVar RCV Id: RCV000040942 RCV000172455 RCV000544021 RCV000769101 RCV002371853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn3225Ser
CA141678
NM_001267550.2:c.9674A>G