Canonical Allele Identifier: PA296907
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1677His
CA015595
NM_000257.4:c.5030G>A