Canonical Allele Identifier: PA2828319306
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 177722
ClinVar RCV Id: RCV000154329 RCV000674570 RCV001073538 RCV001224495 RCV001831960 RCV003330513
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Gly14Arg
CA278727
NM_001369365.1:c.40G>A
CA381926285
NM_001369365.1:c.40G>C