Canonical Allele Identifier: PA2828319637
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 990561
ClinVar RCV Id: RCV001278609
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Ala312Gly
CA381933210
NM_001369365.1:c.935C>G