Canonical Allele Identifier: PA2829443862
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332704
ClinVar RCV Id: RCV000273760 RCV000296140 RCV000344102 RCV000375299 RCV000331164 RCV000594505 RCV000621517 RCV003226282
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Trp24257Cys
CA1986096
NM_003319.4:c.72771G>T
CA349427059
NM_003319.4:c.72771G>C