Canonical Allele Identifier: PA296768
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys184Gln
CA016180
NM_000257.4:c.550A>C