Canonical Allele Identifier: PA184854
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 179655
ClinVar RCV Id: RCV000156451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1402Lys
CA014639
NM_000257.4:c.4204G>A