Canonical Allele Identifier: PA2825116534
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2147174
ClinVar RCV Id: RCV003077055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Ile1171Met
CA381946839
NM_000260.4:c.3513C>G