Canonical Allele Identifier: PA098235
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu927Lys
CA013043
NM_000257.4:c.2779G>A