Canonical Allele Identifier: PA2830229068
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192088

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ala1160Ser
CA238299
NM_133437.4:c.3478G>T