Canonical Allele Identifier: PA139532
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46924
ClinVar RCV Id: RCV000040194 RCV000228887 RCV000725460 RCV001798148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu10667Lys
CA139530
NM_133378.4:c.31999G>A