Canonical Allele Identifier: PA178646
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165933
ClinVar RCV Id: RCV000152270 RCV000765563 RCV000474565 RCV000618262 RCV001704100 RCV003227676 RCV004532695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.His19976Tyr
CA178643
NM_001267550.2:c.59926C>T