Canonical Allele Identifier: PA178629
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165911
ClinVar RCV Id: RCV000152262 RCV000981791 RCV003137654 RCV002453495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg21022His
CA178627
NM_001267550.2:c.63065G>A