Canonical Allele Identifier: PA140898
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47403
ClinVar RCV Id: RCV000040673 RCV000643291 RCV001697136
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val27286Ile
CA140895
NM_001267550.2:c.81856G>A