Canonical Allele Identifier: PA2825112118
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3074765
ClinVar RCV Id: RCV004014299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu995Lys
CA389046337
NM_000257.4:c.2983G>A