Canonical Allele Identifier: PA132258
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 43187
ClinVar RCV Id: RCV000036091 RCV000724180 RCV000988606 RCV001110090 RCV001114121 RCV001276694 RCV001526685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Arg873Trp
CA132257
NM_000260.4:c.2617C>T