Canonical Allele Identifier: PA2829438115
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202845
ClinVar RCV Id: RCV000472425 RCV001704917 RCV002336482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Thr15211Ser
CA310463
NM_003319.4:c.45631A>T
CA349645266
NM_003319.4:c.45632C>G