Canonical Allele Identifier: PA310127
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_001254479.2:p.Gly19466Ala
CA310125
NM_001267550.2:c.58397G>C