Canonical Allele Identifier: PA181576
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 167756
ClinVar RCV Id: RCV000154873 RCV000289664 RCV000336674 RCV000284033 RCV000376165 RCV000405890 RCV000342470 RCV000617769 RCV001085767 RCV000723860 RCV001798491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Met34251Val
CA181573
NM_001267550.2:c.102751A>G