Canonical Allele Identifier: PA658659132
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 454380
ClinVar RCV Id: RCV000536229
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1582del
CA658658244
NM_000257.4:c.4744_4746del