Canonical Allele Identifier: PA1139676574
Gene: MYO7A HGNC NCBI

Linked Data

ClinVar Variation Id: 991570
ClinVar RCV Id: RCV001279803

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000251.3:p.Phe1597Leu
CA381950935
NM_000260.4:c.4789T>C
CA381950939
NM_000260.4:c.4791C>A
CA381950940
NM_000260.4:c.4791C>G