Canonical Allele Identifier: PA184578
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179517
ClinVar RCV Id: RCV000156307 RCV000529644 RCV002408696 RCV003137678 RCV003486707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu34972Lys
CA184576
NM_001267550.2:c.104914G>A