Canonical Allele Identifier: PA177040
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 164377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly389Glu
CA010316
NM_000257.4:c.1166G>A