Canonical Allele Identifier: PA1139686607
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 945244
ClinVar RCV Id: RCV001215836
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Tyr34786Cys
CA349411918
NM_001267550.2:c.104357A>G