Canonical Allele Identifier: PA309558
Gene: TTN HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asn9411Ser
CA309557
NM_001256850.1:c.28232A>G