Canonical Allele Identifier: PA182013
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178276
ClinVar RCV Id: RCV000155017 RCV000232642 RCV000619102 RCV000724953 RCV001131195 RCV001131196 RCV001131197 RCV001131198 RCV001131199
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala445Thr
CA182011
NM_001267550.2:c.1333G>A