Canonical Allele Identifier: PA181602
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178165
ClinVar RCV Id: RCV000154884 RCV000643170 RCV000726736 RCV002372013
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg32548Cys
CA181600
NM_001267550.2:c.97642C>T