Canonical Allele Identifier: PA2828319995
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 2731544
ClinVar RCV Id: RCV003580039
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356294.1:p.Met611Leu
CA6197629
NM_001369365.1:c.1831A>T
CA381938436
NM_001369365.1:c.1831A>C