Canonical Allele Identifier: PA2826421198
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 502402

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala21748Gly
CA349664518
NM_001256850.1:c.65243C>G