Canonical Allele Identifier: PA2829445270
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1479779
ClinVar RCV Id: RCV001976919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg25742Ser
CA349411769
NM_003319.4:c.77226A>T
CA349411770
NM_003319.4:c.77226A>C