Canonical Allele Identifier: PA2830139007
Gene: MMAB HGNC NCBI
ClinVar RCV:
RCV004527209
ClinVar Variation:
3233929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443077.1:p.Arg190Pro
CA386636846
NM_052845.4:c.569G>C