Canonical Allele Identifier: PA2573169926
Gene: AMH HGNC NCBI

Linked Data

ClinVar Variation Id: 1501832
ClinVar RCV Id: RCV002010823

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000470.3:p.Ala530Val
CA9063122
NM_000479.5:c.1589C>T