Canonical Allele Identifier: PA2825113198
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1915560
ClinVar RCV Id: RCV002601577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1663Thr
CA389037193
NM_000257.4:c.4987G>A