Canonical Allele Identifier: PA244759
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 196935
ClinVar RCV Id: RCV000177824 RCV000724089 RCV001272798 RCV004539661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Asn1586Ser
CA244758
NM_000260.4:c.4757A>G