Canonical Allele Identifier: PA645411685
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_001254479.2:p.Gly28714Arg
CA1988548
NM_001267550.2:c.86140G>A
CA349546297
NM_001267550.2:c.86140G>C