Canonical Allele Identifier: PA2830196908
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202735
ClinVar RCV Id: RCV000184654 RCV000387758 RCV000274852 RCV000330015 RCV000335906 RCV000375191 RCV000765567 RCV003317135 RCV002321742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Gly16898Ala
CA310125
NM_133378.4:c.50693G>C