Allele Registry

Canonical Allele Identifier: PA915955614

Gene: AMH HGNC NCBI

ClinVar RCV:

RCV000609747

RCV002066914

ClinVar Variation:

518296

HGVS (amino-acid)	Matching Registered Transcripts
NP_000470.3:p.Ser49Ile	CA9062748 NM_000479.5:c.146G>T