Canonical Allele Identifier: PA311478
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 74312
ClinVar RCV Id: RCV000185190 RCV000535408 RCV000620633 RCV000734888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu2571Lys
CA311474
NM_001267550.2:c.7711G>A