Canonical Allele Identifier: PA915955614
Gene: AMH HGNC NCBI

Linked Data

ClinVar Variation Id: 518296
ClinVar RCV Id: RCV000609747 RCV002066914
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Amino-acid Alleles

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