Canonical Allele Identifier: PA645409629
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238765
ClinVar RCV Id: RCV000239005 RCV000232547 RCV001086491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro12968Ser
CA1996964
NM_001267550.2:c.38902C>T