Canonical Allele Identifier: PA2829443607
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165678
ClinVar RCV Id: RCV000152169 RCV000462130 RCV000620518 RCV000764303 RCV001701771 RCV004532688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Met23891Val
CA178391
NM_003319.4:c.71671A>G