Canonical Allele Identifier: PA2826426267
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 586909
ClinVar RCV Id: RCV000714126

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu30366Gly
CA349454837
NM_001256850.1:c.91097A>G