Canonical Allele Identifier: PA207834
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 212459
ClinVar RCV Id: RCV000193980 RCV002485292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu33342Lys
CA207833
NM_133378.4:c.100024G>A