Canonical Allele Identifier: PA309901
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202659
ClinVar RCV Id: RCV000184558 RCV000728010 RCV002503727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser15946Pro
CA309899
NM_001267550.2:c.47836T>C