Canonical Allele Identifier: PA139452
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46895
ClinVar RCV Id: RCV000040165 RCV000261380 RCV000315424 RCV000353902 RCV000264717 RCV000300081 RCV000643124 RCV000714019 RCV001170394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu10969Lys
CA139449
NM_001256850.1:c.32905G>A