Canonical Allele Identifier: PA2829441315
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191861
ClinVar RCV Id: RCV000172211 RCV002354434 RCV002478554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Thr20531Ser
CA237725
NM_003319.4:c.61592C>G
CA349524843
NM_003319.4:c.61591A>T