Canonical Allele Identifier: PA2826427868
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 466707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Met32610Lys
CA1985710
NM_001256850.1:c.97829T>A