Canonical Allele Identifier: PA2825112206
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2663795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1075Glu
CA257817897
NM_000257.4:c.3223C>G