Allele Registry

Canonical Allele Identifier: PA645435179

Gene: MMUT HGNC NCBI

ClinVar RCV:

RCV000489403

ClinVar Variation:

427056

HGVS (amino-acid)	Matching Registered Transcripts
NP_000246.2:p.Ser306Tyr	CA364401067 NM_000255.4:c.917C>A