Canonical Allele Identifier: PA916066050
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 281858
ClinVar RCV Id: RCV000356393 RCV000643757 RCV001293196 RCV002487189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Val7461Met
CA1994710
NM_133437.4:c.22381G>A