Canonical Allele Identifier: PA2741849726
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 3027063
ClinVar RCV Id: RCV003887456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly35425Arg
CA1985138
NM_001267550.2:c.106273G>C
CA349406365
NM_001267550.2:c.106273G>A