Canonical Allele Identifier: PA2825114683
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 1926695
ClinVar RCV Id: RCV002630793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Lys203Asn
CA381932047
NM_000260.4:c.609G>C
CA381932048
NM_000260.4:c.609G>T