Canonical Allele Identifier: PA310432
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202834
ClinVar RCV Id: RCV000184786 RCV001508108 RCV002503734 RCV002327004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr23875Asn
CA310430
NM_001267550.2:c.71624C>A