Canonical Allele Identifier: PA2829439788
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332761
ClinVar RCV Id: RCV000261667 RCV000315436 RCV000319078 RCV000354170 RCV000368850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Gly18110Ser
CA1989198
NM_003319.4:c.54328G>A