Canonical Allele Identifier: PA2830195596
Gene: TTN HGNC NCBI
ClinVar RCV:
RCV002275541
ClinVar Variation:
1701398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ile13690Val
CA349608043
NM_133378.4:c.41068A>G