Canonical Allele Identifier: PA2826491613
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229404
ClinVar RCV Id: RCV000218656 RCV000643227 RCV001560262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly736Arg
CA10576581
NM_001267550.2:c.2206G>A
CA349501068
NM_001267550.2:c.2206G>C