Canonical Allele Identifier: PA184090
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 179272

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala381Thr
CA010273
NM_000257.4:c.1141G>A