Canonical Allele Identifier: PA2826416271
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp12639Gly
CA237989
NM_001256850.1:c.37916A>G