Canonical Allele Identifier: PA2825186189
Gene: AMH HGNC NCBI

Linked Data

ClinVar Variation Id: 3065466
ClinVar RCV Id: RCV003990543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000470.3:p.Ter561Cys
CA403243906
NM_000479.5:c.1683A>C
CA403243908
NM_000479.5:c.1683A>T