Canonical Allele Identifier: PA645412742
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238694

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala34672Val
CA1985501
NM_001267550.2:c.104015C>T