Canonical Allele Identifier: PA645411458
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332755
ClinVar RCV Id: RCV000267737 RCV000268849 RCV000322601 RCV000328564 RCV000363314 RCV000554942 RCV001170782 RCV001565800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val27761Leu
CA1988947
NM_001267550.2:c.83281G>C