Canonical Allele Identifier: PA2826420675
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu20800Gly
CA237855
NM_001256850.1:c.62399A>G