Canonical Allele Identifier: PA2573062858
Gene: AMH HGNC NCBI

Linked Data

ClinVar Variation Id: 1307724
ClinVar RCV Id: RCV001772579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000470.3:p.Arg522Pro
CA403243501
NM_000479.5:c.1565G>C