Canonical Allele Identifier: PA2826428969
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 2921699
ClinVar RCV Id: RCV003782721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly33699Val
CA349407206
NM_001256850.1:c.101096G>T