Canonical Allele Identifier: PA311351
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203129
ClinVar RCV Id: RCV000542098 RCV001704944 RCV003150077 RCV002327010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala1430Glu
CA311349
NM_001256850.1:c.4289C>A