Canonical Allele Identifier: PA645427319
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 306181
ClinVar RCV Id: RCV000266912 RCV000324370 RCV000376712 RCV001375357 RCV001279411 RCV001239326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Ala1005Val
CA224841733
NM_000260.4:c.3014C>T