Canonical Allele Identifier: PA296656
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181248

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1400Gly
CA014630
NM_000257.4:c.4199C>G