Canonical Allele Identifier: PA916065794
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Pro7106Leu
CA237963
NM_133437.4:c.21317C>T