Canonical Allele Identifier: PA658815177
Gene: TTN HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly21395Ala
CA1991938
NM_001267550.2:c.64184G>C