Canonical Allele Identifier: PA183627
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179052
ClinVar RCV Id: RCV000155836 RCV000725087 RCV001084589 RCV003486701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro11280Ser
CA183625
NM_001267550.2:c.33838C>T