Canonical Allele Identifier: PA309083
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gly21269Arg
CA309082
NM_001256850.1:c.63805G>A
CA349671294
NM_001256850.1:c.63805G>C