Canonical Allele Identifier: PA2825115733
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2503060
ClinVar RCV Id: RCV003389521
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Gln698Arg
CA381939584
NM_000260.4:c.2093A>G