Canonical Allele Identifier: PA3068371728
Gene: MYNN HGNC NCBI
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061127.1:p.His6Gln
CA355057331
NM_018657.5:c.18C>A
CA355057333
NM_018657.5:c.18C>G