Allele Registry

Canonical Allele Identifier: PA1139673820

Gene: MYH7 HGNC NCBI

ClinVar Variation Id: 864287

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Met1046Arg	CA035837 NM_000257.4:c.3137T>G