Canonical Allele Identifier: PA2830234198
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202795
ClinVar RCV Id: RCV000262020 RCV000298416 RCV000406787 RCV000557186 RCV000341773 RCV000356447 RCV001721159 RCV002354501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ala12966Thr
CA310313
NM_133437.4:c.38896G>A