Canonical Allele Identifier: PA2829445837
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2016721
ClinVar RCV Id: RCV002851719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Thr26276Ser
CA349407201
NM_003319.4:c.78827C>G
CA349407203
NM_003319.4:c.78826A>T