Canonical Allele Identifier: PA309662
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202582
ClinVar RCV Id: RCV000184463 RCV000307624 RCV000347083 RCV000301950 RCV000392883 RCV000215227 RCV000400273 RCV000553458 RCV002408817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Glu356Gln
CA309658
NM_133379.5:c.1066G>C