Canonical Allele Identifier: PA296782
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181321

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys246Arg
CA016736
NM_000257.4:c.737A>G