Allele Registry

Canonical Allele Identifier: PA2499232728

Gene: AMH HGNC NCBI

ClinVar Allele:

1164546

ClinVar RCV:

RCV001528928

RCV002070352

ClinVar Variation:

1174814

HGVS (amino-acid)	Matching Registered Transcripts
NP_000470.3:p.Val515Ala	CA9063106 NM_000479.5:c.1544T>C