Canonical Allele Identifier: PA2825115702
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2849875
ClinVar RCV Id: RCV003688039

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Phe678Leu
CA381939379
NM_000260.4:c.2032T>C
CA381939386
NM_000260.4:c.2034C>A
CA381939387
NM_000260.4:c.2034C>G