Canonical Allele Identifier: PA138842
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46643
ClinVar RCV Id: RCV000039913 RCV000172695 RCV000335088 RCV000370482 RCV000313481 RCV000390068 RCV000394105 RCV001087573 RCV001170641 RCV004545740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp6249Asn
CA138838
NM_001267550.2:c.18745G>A