Canonical Allele Identifier: PA2829429889
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535063
ClinVar RCV Id: RCV000642830 RCV002440296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Phe943Leu
CA2005674
NM_003319.4:c.2829C>A
CA349491103
NM_003319.4:c.2829C>G
CA349491153
NM_003319.4:c.2827T>C