Canonical Allele Identifier: PA2573165105
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1361727
ClinVar RCV Id: RCV001899824

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1064Lys
CA389045259
NM_000257.4:c.3190G>A