Canonical Allele Identifier: PA278723
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 164693
ClinVar RCV Id: RCV000151505 RCV000844721 RCV001214273 RCV001808416
ClinVar Variation Id: 2995600
ClinVar RCV Id: RCV003853687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Gly1298Arg
CA278722
NM_000260.4:c.3892G>A
CA381947894
NM_000260.4:c.3892G>C