Canonical Allele Identifier: PA2828321049
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_001356294.1:p.Lys1527Arg
CA381950804
NM_001369365.1:c.4580A>G