Canonical Allele Identifier: PA310219
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202766
ClinVar RCV Id: RCV000276032 RCV000362515 RCV000322078 RCV000376658 RCV000307778 RCV001293203 RCV002460055 RCV001704912
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Phe19358Val
CA310218
NM_001256850.1:c.58072T>G