Canonical Allele Identifier: PA1139675118
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 924864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1632Thr
CA044125
NM_000257.4:c.4894G>A