Canonical Allele Identifier: PA2825109155
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1761860

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu269Gly
CA389052005
NM_000257.4:c.806A>G