Canonical Allele Identifier: PA310027
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202701
ClinVar RCV Id: RCV000184608 RCV000272854 RCV000315949 RCV000330284 RCV000369576 RCV000365027 RCV002433825 RCV003884380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.His17565Asp
CA310025
NM_001267550.2:c.52693C>G