Canonical Allele Identifier: PA2826410820
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ile1595Ser
CA60978210
NM_001256850.1:c.4784T>G