Canonical Allele Identifier: PA2580117814
Gene: AMH HGNC NCBI

Linked Data

ClinVar Variation Id: 2095196
ClinVar RCV Id: RCV003013737
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000470.3:p.Ala554Thr
CA403243820
NM_000479.5:c.1660G>A