Canonical Allele Identifier: PA296930
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181406
ClinVar RCV Id: RCV000158887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met439Arg
CA010528
NM_000257.4:c.1316T>G