Canonical Allele Identifier: PA183133
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178836
ClinVar RCV Id: RCV000155608 RCV000536562 RCV001719976 RCV002453515
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg20367Trp
CA183130
NM_001267550.2:c.61099C>T