Canonical Allele Identifier: PA312068
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203333
ClinVar RCV Id: RCV000185441 RCV000468163 RCV001136403 RCV001136404 RCV001136400 RCV001136402 RCV001136401 RCV001293230 RCV004539730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg8039Cys
CA312067
NM_001256850.1:c.24115C>T