Canonical Allele Identifier: PA2825112331
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1732005
ClinVar RCV Id: RCV002459091

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1167Ser
CA389043685
NM_000257.4:c.3499C>A