Canonical Allele Identifier: PA2826427105
Gene: TTN HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gln31699Lys
CA1986088
NM_001256850.1:c.95095C>A