Canonical Allele Identifier: PA177052
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 164391
ClinVar RCV Id: RCV000151307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile248Phe
CA016758
NM_000257.4:c.742A>T