Canonical Allele Identifier: PA296884
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu987Lys
CA013234
NM_000257.4:c.2959G>A