Canonical Allele Identifier: PA181736
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178194
ClinVar RCV Id: RCV000154924 RCV000226257 RCV001561005 RCV002326884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu23285Lys
CA181734
NM_001267550.2:c.69853G>A