Canonical Allele Identifier: PA645411022
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229517
ClinVar RCV Id: RCV000214060 RCV000277330 RCV000312104 RCV000369619 RCV000400221 RCV000325463 RCV000474321 RCV000731447 RCV002338688 RCV003448289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp25164Asn
CA1990042
NM_001267550.2:c.75490G>A