Canonical Allele Identifier: PA2830204869
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466773
ClinVar RCV Id: RCV000542507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile33379Val
CA349398739
NM_133378.4:c.100135A>G