Canonical Allele Identifier: PA2580176996
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2031504
ClinVar RCV Id: RCV002867259

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gln34781His
CA349411948
NM_001267550.2:c.104343G>T
CA349411949
NM_001267550.2:c.104343G>C