Canonical Allele Identifier: PA311762
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203234
ClinVar RCV Id: RCV000464161 RCV001704950 RCV002381621 RCV003233492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys4401Glu
CA311761
NM_001256850.1:c.13201A>G