Canonical Allele Identifier: PA138914
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46670
ClinVar RCV Id: RCV000039940 RCV000082369 RCV001086508 RCV001798133 RCV001132885 RCV001132886 RCV001132887 RCV001132888 RCV001132889 RCV004541135
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ser5535Cys
CA138912
NM_133378.4:c.16603A>T