Canonical Allele Identifier: PA2825113019
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1709419
ClinVar RCV Id: RCV003320268

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1564Ala
CA389037849
NM_000257.4:c.4691A>C