Canonical Allele Identifier: PA1139745781
Gene: TTN HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Leu3278Val
CA349674296
NM_133379.5:c.9832C>G