Canonical Allele Identifier: PA206734
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203242
ClinVar RCV Id: RCV000193330 RCV000550893 RCV000852915 RCV001706160
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Cys4654Gly
CA206732
NM_001256850.1:c.13960T>G