Canonical Allele Identifier: PA311789
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203244
ClinVar RCV Id: RCV000185330 RCV000727794 RCV001087897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser4745Asn
CA311788
NM_001256850.1:c.14234G>A