Canonical Allele Identifier: PA2826426491
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47580
ClinVar RCV Id: RCV000040849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile30730Val
CA141413
NM_001256850.1:c.92188A>G