Canonical Allele Identifier: PA658827618
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 560716
ClinVar RCV Id: RCV000678977

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu924Gly
CA389047110
NM_000257.4:c.2771A>G