Canonical Allele Identifier: PA181678
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_001254479.2:p.Gln28506Lys
CA181675
NM_001267550.2:c.85516C>A