Canonical Allele Identifier: PA139377
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46858
ClinVar RCV Id: RCV000040128 RCV000233950 RCV000725168 RCV001134533 RCV001134534 RCV001134535 RCV001135959 RCV001135960 RCV004528207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro10613Ala
CA139375
NM_001267550.2:c.31837C>G