Canonical Allele Identifier: PA096616
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 218992
ClinVar RCV Id: RCV000203354 RCV001853275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Tyr231Asn
CA347881
NM_000255.4:c.691T>A