Canonical Allele Identifier: PA312012
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203314
ClinVar RCV Id: RCV000467240 RCV001135645 RCV001135646 RCV001135648 RCV000727733 RCV001135647 RCV001135649
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gln7480Pro
CA312010
NM_001267550.2:c.22439A>C