Canonical Allele Identifier: PA183499
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179010
ClinVar RCV Id: RCV000155789 RCV000184979 RCV000249201 RCV001080345 RCV000769879 RCV004535000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala30548Val
CA183496
NM_001267550.2:c.91643C>T