Canonical Allele Identifier: PA2830206832
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 448774
ClinVar RCV Id: RCV000517328 RCV000525218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr6018Ser
CA2000953
NM_133378.4:c.18053C>G
CA349531614
NM_133378.4:c.18052A>T