Canonical Allele Identifier: PA2828291201
Gene: MYO6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2986681
ClinVar RCV Id: RCV003846336
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001355795.1:p.Pro1174Ser
CA141060202
NM_001368866.1:c.3520C>T