Canonical Allele Identifier: PA309122
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202334
ClinVar RCV Id: RCV000184176 RCV000470417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg29211His
CA309120
NM_001267550.2:c.87632G>A