Canonical Allele Identifier: PA2830200802
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 437103
ClinVar RCV Id: RCV000503192 RCV000553043 RCV000732209
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly26146Arg
CA1988548
NM_133378.4:c.78436G>A
CA349546297
NM_133378.4:c.78436G>C