Canonical Allele Identifier: PA645409297
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 287945
ClinVar RCV Id: RCV000382422 RCV001131908 RCV001131909 RCV001131910 RCV001131911 RCV001129214
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Lys8554Glu
CA2000162
NM_001267550.2:c.25660A>G