Canonical Allele Identifier: PA141667
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47669
ClinVar RCV Id: RCV000040938 RCV000291584 RCV000344090 RCV000292859 RCV000350073 RCV000388022 RCV000474765 RCV000618932 RCV001703917 RCV004537120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu32221Lys
CA141665
NM_133378.4:c.96661G>A