Canonical Allele Identifier: PA2830238767
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47473

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Gly20491Ser
CA141118
NM_133437.4:c.61471G>A