Canonical Allele Identifier: PA139297
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46827
ClinVar RCV Id: RCV000040097 RCV000172684 RCV001078743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala9663Thr
CA139294
NM_001256850.1:c.28987G>A