Canonical Allele Identifier: PA2830209207
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr27650Ala
CA1987762
NM_133378.4:c.82948A>G