Canonical Allele Identifier: PA2499230266
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1007310
ClinVar RCV Id: RCV001304467

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1051Glu
CA389045365
NM_000257.4:c.3152C>A