Canonical Allele Identifier: PA658804611
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 500416
ClinVar RCV Id: RCV000591647 RCV001074974 RCV001829663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Gly1982Arg
CA6198875
NM_000260.4:c.5944G>A
CA381933889
NM_000260.4:c.5944G>C