Canonical Allele Identifier: PA181677
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178180
ClinVar RCV Id: RCV000154907 RCV000621827 RCV000543680 RCV001132347 RCV001132346 RCV001132343 RCV001132344 RCV001132345 RCV001704124 RCV004534970
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gln26865Lys
CA181675
NM_001256850.1:c.80593C>A