Canonical Allele Identifier: PA276013
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 208597
ClinVar RCV Id: RCV000190606 RCV000211873 RCV000223729 RCV001179058 RCV001852531 RCV002354537
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1344Gln
CA276011
NM_000257.4:c.4031G>A