Canonical Allele Identifier: PA183911
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179187
ClinVar RCV Id: RCV000155973 RCV000172667 RCV000242630 RCV001135859 RCV001085935 RCV001128852 RCV001128853 RCV001135860 RCV001135861 RCV004535005
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp14477Gly
CA183909
NM_001256850.1:c.43430A>G