Canonical Allele Identifier: PA2741835093
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2891552
ClinVar RCV Id: RCV003723011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Leu625Pro
CA381938467
NM_001127180.2:c.1874T>C