Allele Registry

Canonical Allele Identifier: PA2828321785

Gene: MYO7A HGNC NCBI

ClinVar Allele:

431768

ClinVar RCV:

RCV000504907

RCV001857218

ClinVar Variation:

438179

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356294.1:p.Thr2135Met	CA381938356 NM_001369365.1:c.6404C>T