Canonical Allele Identifier: PA2830204432
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 851369
ClinVar RCV Id: RCV001055752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser32784Cys
CA60953460
NM_133378.4:c.98351C>G