Canonical Allele Identifier: PA184843
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179648
ClinVar RCV Id: RCV000156444 RCV000475607 RCV000620906 RCV003149957 RCV001262303 RCV004535009 RCV003137680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala34754Val
CA184841
NM_001267550.2:c.104261C>T