Canonical Allele Identifier: PA2741849463
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2691065
ClinVar RCV Id: RCV003487128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Cys9195Ser
CA1999780
NM_001267550.2:c.27584G>C
CA349451032
NM_001267550.2:c.27583T>A