Canonical Allele Identifier: PA178876
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166082
ClinVar RCV Id: RCV000152360 RCV000228409 RCV001704102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu10759Gly
CA178875
NM_133378.4:c.32276A>G