Canonical Allele Identifier: PA2830226555
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1479779
ClinVar RCV Id: RCV001976919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Arg25867Ser
CA349411769
NM_133432.3:c.77601A>T
CA349411770
NM_133432.3:c.77601A>C