Canonical Allele Identifier: PA309756
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202613
ClinVar RCV Id: RCV000184499 RCV000643131 RCV000622210 RCV003137715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr11958Ile
CA309755
NM_001256850.1:c.35873C>T