Canonical Allele Identifier: PA178645
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165933
ClinVar RCV Id: RCV000152270 RCV000765563 RCV000474565 RCV000618262 RCV001704100 RCV003227676 RCV004532695
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.His18335Tyr
CA178643
NM_001256850.1:c.55003C>T