Canonical Allele Identifier: PA2828320059
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1067673
ClinVar RCV Id: RCV001379002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Arg657Pro
CA6197661
NM_001369365.1:c.1970G>C