Canonical Allele Identifier: PA2826489490
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467418
ClinVar RCV Id: RCV000770125 RCV002367862 RCV001824822 RCV000546592 RCV001567645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg2317His
CA2004933
NM_001267550.2:c.6950G>A