Canonical Allele Identifier: PA140949
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47422
ClinVar RCV Id: RCV000040692 RCV000171313 RCV000466706 RCV000769925 RCV001330312 RCV002345321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val26120Ile
CA140946
NM_001256850.1:c.78358G>A