Canonical Allele Identifier: PA309972
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202683
ClinVar RCV Id: RCV000184587 RCV000993449 RCV000471332 RCV002444750 RCV003335182 RCV003486749
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu15097Lys
CA309971
NM_001256850.1:c.45289G>A