Canonical Allele Identifier: PA2580117779
Gene: AMH HGNC NCBI

Linked Data

ClinVar Variation Id: 2490212
ClinVar RCV Id: RCV003220246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000470.3:p.Trp438Leu
CA403242747
NM_000479.5:c.1313G>T