Canonical Allele Identifier: PA312711
Gene: MMAB HGNC NCBI

Linked Data

ClinVar Variation Id: 203817

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443077.1:p.Thr62Met
CA312710
NM_052845.4:c.185C>T