Canonical Allele Identifier: PA915957159
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773940
ClinVar RCV Id: RCV003532702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1023Thr
CA389045726
NM_000257.4:c.3067G>A