Canonical Allele Identifier: PA645414686
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 372429

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala226Thr
CA16042915
NM_000257.4:c.676G>A