Canonical Allele Identifier: PA178966
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166152
ClinVar RCV Id: RCV000152397 RCV000172383 RCV000346191 RCV000284465 RCV000376603 RCV000345184 RCV000391562 RCV001086487 RCV003149931 RCV004544374
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val8001Ile
CA178964
NM_001256850.1:c.24001G>A