Canonical Allele Identifier: PA310207
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp19170Gly
CA310206
NM_001256850.1:c.57509A>G