Allele Registry

Canonical Allele Identifier: PA658804418

Gene: MYH7 HGNC NCBI

ClinVar RCV:

RCV000614191

ClinVar Variation:

505562

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Arg403Gly	CA389051122 NM_000257.4:c.1207C>G