Canonical Allele Identifier: PA237667
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191837
ClinVar RCV Id: RCV000172178 RCV000213432 RCV000284749 RCV000339727 RCV000278672 RCV000343230 RCV000393696 RCV000527211 RCV002362883 RCV004535170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro32881Ser
CA237665
NM_001267550.2:c.98641C>T