Canonical Allele Identifier: PA140551
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47279
ClinVar RCV Id: RCV000726999 RCV001088941 RCV003149656 RCV000040549 RCV000246349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val23302Ile
CA140548
NM_001267550.2:c.69904G>A