Canonical Allele Identifier: PA2499230359
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1171923
ClinVar RCV Id: RCV001525385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1584Gly
CA043766
NM_000257.4:c.4751A>G