Canonical Allele Identifier: PA2830226899
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile26191Val
CA311220
NM_133432.3:c.78571A>G