Canonical Allele Identifier: PA2825115214
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1351867
ClinVar RCV Id: RCV002047168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Lys502Asn
CA6197504
NM_000260.4:c.1506G>T
CA381935671
NM_000260.4:c.1506G>C