Canonical Allele Identifier: PA296678
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181261

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1555Gly
CA015211
NM_000257.4:c.4664A>G