Canonical Allele Identifier: PA183579
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179036
ClinVar RCV Id: RCV000155820 RCV000260975 RCV000262328 RCV000316313 RCV000322180 RCV000375521 RCV000542437 RCV000726570 RCV003149949 RCV002415668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala35607Val
CA183576
NM_001267550.2:c.106820C>T