Canonical Allele Identifier: PA645431589
Gene: MYO6 HGNC NCBI

Linked Data

ClinVar Variation Id: 397508
ClinVar RCV Id: RCV000449594
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004990.3:p.Val183Asp
CA16609392
NM_004999.4:c.548T>A