Canonical Allele Identifier: PA645510099
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 438177
ClinVar RCV Id: RCV000505067 RCV000670174 RCV001047383
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Asn1182Lys
CA381946913
NM_000260.4:c.3546C>A
CA381946914
NM_000260.4:c.3546C>G