Canonical Allele Identifier: PA140894
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47401
ClinVar RCV Id: RCV000040671 RCV000643828 RCV000727800 RCV001170785 RCV004541180 RCV002345315
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn27224Ser
CA140891
NM_001267550.2:c.81671A>G