Canonical Allele Identifier: PA2825115226
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1905172
ClinVar RCV Id: RCV002592873
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Leu509Phe
CA381935743
NM_000260.4:c.1525C>T