Canonical Allele Identifier: PA311864
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203266
ClinVar RCV Id: RCV000228104 RCV000769074 RCV001508479
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Tyr6013His
CA311862
NM_001267550.2:c.18037T>C