Canonical Allele Identifier: PA2830225955
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 167756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Met25311Val
CA181573
NM_133432.3:c.75931A>G