Canonical Allele Identifier: PA2830238770
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 196096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Gly20496Val
CA242898
NM_133437.4:c.61487G>T