Canonical Allele Identifier: PA2825112158
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1710269

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1040Arg
CA389045480
NM_000257.4:c.3119A>G