Canonical Allele Identifier: PA2830242886
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1479779
ClinVar RCV Id: RCV001976919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Arg25934Ser
CA349411769
NM_133437.4:c.77802A>T
CA349411770
NM_133437.4:c.77802A>C