Canonical Allele Identifier: PA097996
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 407189

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln222Lys
CA16614501
NM_000257.4:c.664C>A