Canonical Allele Identifier: PA2580117781
Gene: AMH HGNC NCBI

Linked Data

ClinVar Variation Id: 2460062
ClinVar RCV Id: RCV003189517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000470.3:p.Arg441Pro
CA304214099
NM_000479.5:c.1322G>C