Canonical Allele Identifier: PA2580117811
Gene: AMH HGNC NCBI

Linked Data

ClinVar Variation Id: 2038298
ClinVar RCV Id: RCV002890646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000470.3:p.Val553Leu
CA9063141
NM_000479.5:c.1657G>T
CA403243811
NM_000479.5:c.1657G>C