Canonical Allele Identifier: PA2825112130
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1938030
ClinVar RCV Id: RCV002662421

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp1009Gly
CA389045859
NM_000257.4:c.3026A>G