Allele Registry

Canonical Allele Identifier: PA2825112997

Gene: MYH7 HGNC NCBI

ClinVar Allele:

3230999

ClinVar RCV:

RCV004013580

ClinVar Variation:

3072558

HGVS (amino-acid)	Matching Registered Transcripts
NP_000248.2:p.Glu1554Gln	CA043434 NM_000257.4:c.4660G>C