Canonical Allele Identifier: PA916065936
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229442

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ala7280Ser
CA10576523
NM_133437.4:c.21838G>T