Canonical Allele Identifier: PA183132
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_001243779.1:p.Arg18726Trp
CA183130
NM_001256850.1:c.56176C>T