Canonical Allele Identifier: PA2826428970
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2933743
ClinVar RCV Id: RCV003793301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly33699Ala
CA349407207
NM_001256850.1:c.101096G>C