Canonical Allele Identifier: PA2830204005
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1479779
ClinVar RCV Id: RCV001976919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg32239Ser
CA349411769
NM_133378.4:c.96717A>T
CA349411770
NM_133378.4:c.96717A>C