Canonical Allele Identifier: PA2826428378
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_001243779.1:p.Ala33113Val
CA184841
NM_001256850.1:c.99338C>T