Canonical Allele Identifier: PA2830203869
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238694

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala32104Val
CA1985501
NM_133378.4:c.96311C>T