Canonical Allele Identifier: PA915957470
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 660218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1586Thr
CA389037697
NM_000257.4:c.4756G>A