Canonical Allele Identifier: PA237956
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191954
ClinVar RCV Id: RCV000172322 RCV001128751 RCV001128752 RCV001128753 RCV001128754 RCV001135757 RCV001798614
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser16199Pro
CA237954
NM_001267550.2:c.48595T>C