Canonical Allele Identifier: PA311186
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203082
ClinVar RCV Id: RCV000458275 RCV000727494 RCV001170287 RCV002399691
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg34840Gln
CA311184
NM_001267550.2:c.104519G>A