Canonical Allele Identifier: PA2825112670
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1981076
ClinVar RCV Id: RCV002751232

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1406Thr
CA041281
NM_000257.4:c.4216G>A