Canonical Allele Identifier: PA2826414497
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46796

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gln8881Arg
CA139213
NM_001256850.1:c.26642A>G