Canonical Allele Identifier: PA2825108848
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2501805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln193Arg
CA389052497
NM_000257.4:c.578A>G