Canonical Allele Identifier: PA310211
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202763
ClinVar RCV Id: RCV000559556 RCV000726175 RCV001798652 RCV002453680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg20836Gln
CA310209
NM_001267550.2:c.62507G>A