Canonical Allele Identifier: PA309589
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202559

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro10332Ala
CA309587
NM_001267550.2:c.30994C>G