Canonical Allele Identifier: PA2830222177
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Pro20006Ala
CA1988422
NM_133432.3:c.60016C>G