Canonical Allele Identifier: PA645434887
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 357263
ClinVar RCV Id: RCV000670305
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.His14Leu
CA10627106
NM_000255.4:c.41A>T