Canonical Allele Identifier: PA097823
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 177667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg869His
CA012723
NM_000257.4:c.2606G>A