Canonical Allele Identifier: PA312717
Gene: MMAB HGNC NCBI

Linked Data

ClinVar Variation Id: 203819
ClinVar RCV Id: RCV000186018 RCV000203392 RCV001420745
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443077.1:p.Arg190His
CA312716
NM_052845.4:c.569G>A