Canonical Allele Identifier: PA138668
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46584
ClinVar RCV Id: RCV000039854 RCV000172413 RCV000474160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg3486Gln
CA138666
NM_133378.4:c.10457G>A