Canonical Allele Identifier: PA2825112163
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1921562

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp1047His
CA389045408
NM_000257.4:c.3139G>C