Canonical Allele Identifier: PA2828319910
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 143064
ClinVar RCV Id: RCV000132570
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Gly545Val
CA270005
NM_001369365.1:c.1634G>T