Canonical Allele Identifier: PA178967
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166152
ClinVar RCV Id: RCV000152397 RCV000172383 RCV000346191 RCV000284465 RCV000376603 RCV000345184 RCV000391562 RCV001086487 RCV003149931 RCV004544374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val8318Ile
CA178964
NM_001267550.2:c.24952G>A