Canonical Allele Identifier: PA2830205391
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238787
ClinVar RCV Id: RCV000231819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr13198Ser
CA10581867
NM_133378.4:c.39592A>T
CA349618178
NM_133378.4:c.39593C>G