Canonical Allele Identifier: PA270006
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_000251.3:p.Gly556Val
CA270005
NM_000260.4:c.1667G>T