Canonical Allele Identifier: PA645414667
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 407184
ClinVar RCV Id: RCV000467740

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile192Val
CA16614503
NM_000257.4:c.574A>G