Canonical Allele Identifier: PA310464
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202845

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr22635Ser
CA310463
NM_001256850.1:c.67903A>T
CA349645266
NM_001256850.1:c.67904C>G