Canonical Allele Identifier: PA1139676497
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 933867
ClinVar RCV Id: RCV001202169
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Lys1576Arg
CA381950804
NM_000260.4:c.4727A>G