Canonical Allele Identifier: PA2741811978
Gene: MMUT HGNC NCBI

Linked Data

ClinVar Variation Id: 2917762
ClinVar RCV Id: RCV003737850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000246.2:p.Thr170Ser
CA364404578
NM_000255.4:c.509C>G
CA364404579
NM_000255.4:c.508A>T