Canonical Allele Identifier: PA237928
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191941
ClinVar RCV Id: RCV000172308 RCV000219508 RCV000460774 RCV001135752 RCV001135753 RCV001135754 RCV001135750 RCV001135751 RCV002433754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly15898Arg
CA237927
NM_133378.4:c.47692G>A
CA349541761
NM_133378.4:c.47692G>C