Canonical Allele Identifier: PA915981014
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 177732
ClinVar RCV Id: RCV000154342 RCV000406568 RCV000844912 RCV000994688 RCV001003087 RCV000787987 RCV001272505 RCV003152592 RCV004528885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120652.1:p.Ala826Thr
CA180669
NM_001127180.2:c.2476G>A