Canonical Allele Identifier: PA311914
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203283
ClinVar RCV Id: RCV000727008 RCV001132030 RCV001132032 RCV001132033 RCV001132029 RCV001132031
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg6386Gln
CA311913
NM_001256850.1:c.19157G>A