Canonical Allele Identifier: PA140647
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47312
ClinVar RCV Id: RCV000040582 RCV000285232 RCV000334264 RCV000310657 RCV000396450 RCV000403418 RCV001083817 RCV000725033 RCV001170337 RCV002336144 RCV004541174
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu22486Lys
CA140644
NM_001256850.1:c.67456G>A