This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: PA645409738
Gene: TTN HGNC NCBI
ClinVar RCV:
RCV000231378
ClinVar Variation:
238775
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val13965Gly
CA10581873
NM_001267550.2:c.41894T>G