Canonical Allele Identifier: PA138934
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46675
ClinVar RCV Id: RCV000039945 RCV000172393 RCV001081728 RCV001131791 RCV001131792 RCV001129107 RCV001129108 RCV001129109 RCV001170088 RCV004018898
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly6933Ala
CA138930
NM_001267550.2:c.20798G>C