Canonical Allele Identifier: PA2826418436
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys16782Asn
CA140013
NM_001256850.1:c.50346G>C
CA349543218
NM_001256850.1:c.50346G>T