Canonical Allele Identifier: PA2829444403
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165653
ClinVar RCV Id: RCV000152161
ClinVar Variation Id: 535456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Ser24945Arg
CA178372
NM_003319.4:c.74833A>C
CA349418528
NM_003319.4:c.74835T>G
CA349418529
NM_003319.4:c.74835T>A