Canonical Allele Identifier: PA184924
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 179682
ClinVar RCV Id: RCV000156478 RCV001571850 RCV001826852 RCV002515021
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.His253Arg
CA184923
NM_000260.4:c.758A>G