Canonical Allele Identifier: PA183578
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_001243779.1:p.Ala33966Val
CA183576
NM_001256850.1:c.101897C>T